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13q21.31CNV Type: Deletion-Duplication


Largest CNV size: 353828 bp

Statistics Box:
Number of Reports: 12



Summary Information

Summary statement in development

Additional Locus Information

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USCS Symbol             NCBI Symbol

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References

Major Reports

Title
Author, Year
Report Class
CNV Type
Structural variation of chromosomes in autism spectrum disorder.
Deletion
Functional impact of global rare copy number variation in autism spectrum disorders.
Deletion-Duplication

Minor Reports

Title
Author, Year
Report Class
CNV Type
Rare structural variation of synapse and neurotransmission genes in autism.
Deletion-Duplication
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.
Duplication
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Deletion-Duplication
A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Duplication
Global increases in both common and rare copy number load associated with autism.
Duplication
Identification of candidate intergenic risk loci in autism spectrum disorder.
Duplication
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.
Deletion-Duplication
Performance of case-control rare copy number variation annotation in classification of autism.
Deletion-Duplication
Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder.
Duplication
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
Duplication

Cases

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 marshall_08_ASD_discovery_cases
 Cohort of ASD families (237 simplex, 189 mulitplex) recruited from the Hospital for Sick Children, McMaster Univ., Memorial Univ., and other sites
 427
 ASD
 
 
 61837
 1
 0
 1
 pinto_10_ASD_discovery_cases
 Autism Genome Project (AGP) consortium patient cohort from families with at least two ASD individuals
 996
 ASD (ADI-R and ADOS): strict, broad, or spectrum ASD
 
 
 122094
 2
 3
 5
 gai_11_ASD_discovery_cases
 Discovery case samples derived from AGRE set 4 (most recent patient recruitment)
 631
 Idiopathic autism; cases designated as 'spectrum' and 'not quite autism' excluded, as were cases with known genetic syndromes or other non-idiopathic causes
 
 
 126305
 0
 1
 1
 gai_11_ASD_replication_cases
 Replication case samples derived from AGRE sets 1-3
 593
 Idiopathic autism; cases designated as 'spectrum' and 'not quite autism' excluded, as were cases with known genetic syndromes or other non-idiopathic causes
 
 
 108407
 5
 1
 6
 nord_11_ASD_discovery_cases
 Youth with ASD (as part of mother-father-child trios)
 41
 ASD
 
 85.4% Male
 43356
 0
 1
 1
 sanders_11_ASD_discovery_cases
 Autistic probands from the Simons Simplex Collection (SSC). 872 probands in quartet families, 272 probands in trios.
 1124
 ASD diagnosis: 89.5% autism; 8.5% PDD-NOS, 2% Asperger syndrome. Mean full-scale IQ 85.1 ± 1.5 (mean verbal IQ, 81.9 ± 1.7; mean non-verbal IQ, 88.4 ± 1.4)
 Mean, 9.1 yrs.
 86.1% Male
 353828
 7
 6
 13
 prasad_12_ASD_discovery_cases
 Unrelated ASD cases recruited from three Canadian sites (Hospital for Sick Children in Toronto, Ontario; McMaster University, Hamilton, Ontario; Memorial University of Newfoundland, St. John's, Newfoundland); the majority of these cases had been previously genotyped by SNP arrays with results published in Marshall et al., 2008 and Pinto et al., 2010. 20 cases from initial cohort of 696 were exclu
 676
 Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS
 NA
 82.84% Male
 120637
 0
 2
 2
 girirajan_13b_ASD_discovery_cases
 Children with autism ascertained from the Childhood Autism Risks from Genetics and Environment (CHARGE) study conducted through the Medical Investigation of Neurodevelopmental Disorders (MIND) Institute at UC-Davis after passing QC criteria (274 initial cases)
 243
 Diagnosis of autism confirmed by ADOS and ADI-R. Exclusion criteria: children with developmental delay but lacking symptoms and autism, as well as children with ASD as defined by the CHARGE protocol
 N/A
 N/A
 404558
 0
 1
 1
 walker_13_ASD_discovery_cases
 Unrelated ASD probands previously described in Lionel et al., 2011 and Pinto et al., 2010 CNV reports
 1491
 Diagnosis of ASD based on gold-standard instruments including ADI and ADOS.
 N/A
 N/A
 108406
 0
 1
 1
 sajan_13_ACC/CBLH/PMG_discovery_cases
 Individuals with severe congenital brain malformations [agenesis of the corpus callosum (ACC), cerebellar hypoplasia (CBLH), and/or polymicrogyria (PMG)] and additional neurodevelopmental phenotypes
 487
 Diagnosis of agenesis of the corpus callosum (ACC), cerebellar hypoplasia (CBLH), and/or polymicrogyria (PMG); additional diagnoses of autism spectrum disorder (ASD), developmental delay (DD), intellectual disability (ID) and/or seizures in some patients
 N/A
 N/A
 142581
 3
 2
 5
 engchuan_15_ASD_discovery_cases
 Samples from the Autism Genome Project (AGP)
 1892
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 N/A
 85.78% Male
 508469
 9
 7
 16
 mosca_16_DCD_discovery_cases
 Participants recruited as part of a multidisciplinary study at the Alberta Children's Hospital (Calgary, Alberta, Canada)
 82
 All cases met diagnostic criteria for developmental coordination disorder (DCD) with or without co-occurring ADHD and/or reading disorder.
 Range, 8-17 years (Mean, 10.06 ± 2.92 yrs.)
 N/A
 138029
 0
 2
 2
 leppa_16_ASD_discovery_cases
 Children affected with ASD from 1,464 families from the Autism Genetic Resource Exchange (AGRE)
 1764
 Diagnosis according to ADOS and ADI-R
 N/A
 N/A
 700000
 0
 1
 1

Controls

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 marshall_08_ASD_discovery_controls_1
 German PopGen project and entries from Database of Genomic Variants
 500
 Controls
 
 
 0
 0
 0
 0
 marshall_08_ASD_discovery_controls_2
 Non-disease controls from Ontario population
 1152
 Controls
 
 
 0
 0
 0
 0
 nord_11_ASD_discovery_controls
 Samples from 367 total control individuals (319 European American, 48 African American) used to test for differences in rare CNV prevalence compared with autism cases
 123
 Controls (no history of psychiatric symptoms by self-report)
 ? 30 yrs.
 
 0
 0
 0
 0
 sanders_11_ASD_discovery_controls
 Matched siblings of autistic probands from the Simons Simplex Collection (SSC).
 872
 Controls
 Mean, 10.0 yrs.
 
 321321
 12
 6
 18
 levy_11_ASD_discovery_controls
 Unaffected siblings of autistic probands from 887 families from the Simons Simplex Collection (SSC)
 863
 Control
 
 47.97% Male
 314549
 0
 1
 1
 prasad_12_ASD_discovery_controls
 PDx controls [1000 DNA samples from reportedly healthy donors (50.2% male) from BioServe (Beltsville, MD)] and 4139 in-house controls previously reported in Krawcak et al. 2006, Stewart et al. 2009, and Bierut et al. 2010. CNVs identified in controls were used to define rare ASD-specific CNVs.
 5139
 Control
 NA
 NA (PDx controls 50.2% male)
 120637
 0
 0
 0
 girirajan_13b_ASD_discovery_controls
 Controls ascertained from the Childhood Autism Risks from Genetics and Environment (CHARGE) study conducted through the Medical Investigation of Neurodevelopmental Disorders (MIND) Institute at UC-Davis after passing QC criteria (242 initial controls)
 223
 Control
 N/A
 N/A
 0
 0
 0
 0
 walker_13_ASD_discovery_controls
 Control samples from the SAGE cohort (n=1287), from the Ottawa Heart Institute (n=1234), and from the POPGEN collection (n=1123)
 3644
 Control
 N/A
 N/A
 108406
 N/A
 N/A
 N/A
 engchuan_15_ASD_discovery_controls
 Platform-matched controls from three large studies: SAGE (Study of Addiction Genetics and Environment), Ontario Colorectal Cancer study, and HABC (Health Aging and Body Composition)
 2342
 Controls; subjects had no previous psychiatric history
 N/A
 46.67% Male
 523682
 16
 6
 22
 kanduri_15_ASD_discovery_controls
 Unrelated Finnish samples from the cohort of Health 2000 survey from an initial sample of 288 individuals following quality control
 269
 Controls screened for DSM-IV mental disorders using the Composite International Diagnostic Interview and psychotic disorders using the research version of the Structured Clinical Interview for DSM-IV
 N/A
 N/A
 117088
 1
 0
 1

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 marshall_08_ASD_discovery_cases
  90% European, 4.5% European-mixed, 4.5% Asian, 0.07% African
 Array SNP, karotyping
  Affy 500K
 dChip, CNAG, & GEMCA
 
 qPCR, qmPCR
 pinto_10_ASD_discovery_cases
  European
 Solid phase hybridization
  Illumina Infinium 1M SNP microarray
 QuantiSNP & iPattern
 
 qPCR, long-range PCR (LR-PCR), MLPA, FISH, aCGH (Agilent 1M), and/or array SNP (Affy 500K)
 gai_11_ASD_discovery_cases
  European
 Solid phase hybridization
  Illumina Infinium II HumanHap550 BeadChip
 
 BeadStudio 3
 None
 gai_11_ASD_replication_cases
  European
 Solid phase hybridization
  Illumina Infinium II HumanHap550 BeadChip
 
 BeadStudio 3
 None
 nord_11_ASD_discovery_cases
  29 European American, 3 Asian American, 2 Hispanic, 2 African American, 5 unknown ancestry
 aCGH
  NimbleGen HD2
 Sliding-window algorithm, ~10 kb minumum size threshold
 
 None
 sanders_11_ASD_discovery_cases
  White non-Hispanic, 74.5%; mixed, 9.3%, Asian, 4.3%, White Hispanic, 4.0%, African-American, 3.8%; other, 4.2&
 Solid phase hybridization
  Illumina 1M v1 (n=334) or Illumina 1M v3 (n=840)
 PennCNV, QuantiSNP, & GNOSIS
 
 
 prasad_12_ASD_discovery_cases
  Canada
 aCGH
  Agilent 1M
 ADM-2, DNAcopy (R Bioconductor)
 DNA Analytics v4.0.85 (Agilent), DNAcopy
 None
 girirajan_13b_ASD_discovery_cases
  133 European, 57 Hispanic, 27 Mixed Race, 20 Asian, 6 African-American
 aCGH
  Roche NimbleGen custom targeted hotspot array comprised of 135,000 probes with higher density probe coverage in genomic hotspots (regions flanked by segmental duplications)
 DNA Copy Number v1.6
 
 None
 walker_13_ASD_discovery_cases
  N/A
 Solid phase hybridization (n=993) or array SNP (n=498)
  Illumina 1M (n=993) or Affymetrix 6.0 (n=498)
 
 QuantiSNP and PennCNV (Illumina); Birdsuite, iPattern and Genotyping Console for Affymetrix
 None
 sajan_13_ACC/CBLH/PMG_discovery_cases
  81.31% Caucasian
 Solid phase hybridization
  Illumina InfiniumII HumanHap610
 PennCNV
 
 None (not tested or failure to confirm by qPCR)
 engchuan_15_ASD_discovery_cases
  Caucasian
 Solid phase hybridization
  Illumina 1M
 
 
 None
 mosca_16_DCD_discovery_cases
  Canada
 Solid phase hybridization
  Illumina HumanOmni2.5-Quad BeadChip
 iPattern, PennCNV, QuantiSNP, CNVPartition
 
 None
 leppa_16_ASD_discovery_cases
  N/A
 Solid phase hybridization
  Illumina 550v1 and 550v3, Omni-1.0-B and -H, Omni 2.5
 PennCNV, QuantiSNP, GNOSIS
 GenomeStudio, CNVision
 None

Controls

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
  marshall_08_ASD_discovery_controls_1
  European
  Array SNP, karotyping
  Affy 500K
  dChip, CNAG, & GEMCA
 
 
  marshall_08_ASD_discovery_controls_2
  European
  Array SNP, karotyping
  Affy 500K
  dChip, CNAG, & GEMCA
 
 
  nord_11_ASD_discovery_controls
 
  aCGH
  NimbleGen HD2
  Sliding-window algorithm, ~10 kb minumum size threshold
 
  None
  sanders_11_ASD_discovery_controls
 
  Solid phase hybridization
  Illumina 1M v1 or Illumina 1M v3
  PennCNV, QuantiSNP, & GNOSIS
 
 
  levy_11_ASD_discovery_controls
 
  aCGH
  NimbleGen HD2
  HMM
 
 
  prasad_12_ASD_discovery_controls
  NA
  aCGH (PDx controls)
  Agilent 1M (PDx controls)
  PDx controls: ADM-2, DNAcopy (R Bioconductor)
  PDx controls: DNA Analytics v4.0.85 (Agilent), DNAcopy
 
  girirajan_13b_ASD_discovery_controls
  116 European, 70 Hispanic, 27 Mixed Race, 7 Asian, 3 African-American
  aCGH
  Roche NimbleGen custom targeted hotspot array comprised of 135,000 probes with higher density probe coverage in genomic hotspots (regions flanked by segmental duplications)
  DNA Copy Number v1.6
 
 
  walker_13_ASD_discovery_controls
  N/A
  Solid phase hybridization (n=1287) or array SNP (n=2357)
  Illumina 1M (n=1287) or Affymetrix 6.0 (n=2357)
 
  QuantiSNP and PennCNV (Illumina); Birdsuite, iPattern and Genotyping Console for Affymetrix
  None
  engchuan_15_ASD_discovery_controls
  Caucasian
  Solid phase hybridization
  Illumina 1M
 
 
  None
  kanduri_15_ASD_discovery_controls
  Finnish
  Solid phase hybridization
  Illumina Infinium HD Human610-Quad BeadChip
  QuantiSNP, PennCNV
  Illumina BeadStudio
  None

Cases

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  marshall_08_ASD_discovery_cases-NA0028-000
 NA
 M
 ASD
 NA
 NA
 62915912
 62977748
  61837
 NCBI Build35
 Deletion
 Yes
  pinto_10_ASD_discovery_cases-case13094_1113
 NA
 M
 Autism
 Non-verbal
 Normal IQ
 63231043
 63277373
  46331
 
 Duplication
 Yes
  pinto_10_ASD_discovery_cases-case5029_4
 NA
 M
 ASD
 NA
 NA
 63157485
 63268659
  111175
 
 Deletion
 Yes
  pinto_10_ASD_discovery_cases-case5039_4
 NA
 M
 ASD
 NA
 NA
 60567730
 60676136
  108407
 
 Duplication
 Yes
  pinto_10_ASD_discovery_cases-case5213_3
 NA
 M
 ASD
 NA
 NA
 63500894
 63622987
  122094
 
 Duplication
 Yes
  pinto_10_ASD_discovery_cases-case5325_3
 NA
 F
 ASD
 NA
 NA
 63157485
 63271229
  113745
 
 Deletion
 Yes
  gai_11_ASD_discovery_cases-AU1590302
 
 
 Autism
 
 
 63082454
 63208758
  126305
 
 Duplication
 No
  gai_11_ASD_replication_cases-AU070004
 
 
 Autism
 
 
 61666580
 61766720
  100141
 
 Deletion
 No
  gai_11_ASD_replication_cases-AU070005
 
 
 Autism
 
 
 61666580
 61766720
  100141
 
 Deletion
 No
  gai_11_ASD_replication_cases-AU070008
 
 
 Autism
 
 
 61666580
 61766720
  100141
 
 Deletion
 No
  gai_11_ASD_replication_cases-AU071703
 
 
 Autism
 
 
 62104068
 62161921
  57854
 
 Deletion
 No
  gai_11_ASD_replication_cases-AU075503
 
 
 Autism
 
 
 60567730
 60676136
  108407
 
 Duplication
 No
  gai_11_ASD_replication_cases-AU083103
 
 
 Autism
 
 
 62979204
 63010105
  30902
 
 Deletion
 No
  nord_11_ASD_discovery_cases-206-1
 
 
 ASD
 
 
 62010930
 62054285
  43356
 
 Duplication
 No
  sanders_11_ASD_discovery_cases-11027.p1
 9
 M
 ASD
 NA
 Full-scale IQ, 83; non-verbal IQ, 84; verbal IQ, 86
 61996997
 62127880
  130883
 hg18
 Duplication
 No
  sanders_11_ASD_discovery_cases-11121.p1
 10
 M
 Autism
 NA
 Full-scale IQ, 102; non-verbal IQ, 103; verbal IQ, 99
 62104068
 62175177
  71109
 hg18
 Deletion
 No
  sanders_11_ASD_discovery_cases-11145.p1
 5
 M
 Autism
 NA
 Full-scale IQ, 76; non-verbal IQ, 79; verbal IQ 80
 61082769
 61088999
  6230
 hg18
 Deletion
 No
  sanders_11_ASD_discovery_cases-11316.p1
 11
 F
 Autism
 NA
 Full-scale IQ, 47; non-verbal IQ, 45; verbal IQ, 21
 63231043
 63302331
  71288
 hg18
 Duplication
 No
  sanders_11_ASD_discovery_cases-11327.p1
 11
 M
 ASD
 NA
 Full-scale IQ, 84; non-verbal IQ, 86; verbal IQ, 83
 63231043
 63277373
  46330
 hg18
 Duplication
 No
  sanders_11_ASD_discovery_cases-11398.p1
 12
 M
 Autism
 NA
 Full-scale IQ, 94; non-verbal IQ, 106; verbal IQ, 77
 61088375
 61090632
  2257
 hg18
 Deletion
 No
  sanders_11_ASD_discovery_cases-11521.p1
 17
 M
 Autism
 NA
 Full-scale IQ, 111; non-verbal IQ, 101; verbal IQ, 128
 63157485
 63276677
  119192
 hg18
 Deletion
 No
  sanders_11_ASD_discovery_cases-11808.p1
 8
 F
 Autism
 NA
 Full-scale IQ, 84; non-verbal IQ, 81; verbal IQ, 95
 63157485
 63271229
  113744
 hg18
 Deletion
 No
  sanders_11_ASD_discovery_cases-11940.p1
 8
 F
 ASD
 NA
 Full-scale IQ, 114; non-verbal IQ, 109; verbal IQ, 121
 61996997
 62045071
  48074
 hg18
 Duplication
 No
  sanders_11_ASD_discovery_cases-12215.p1
 4
 M
 Autism
 NA
 Full-scale IQ, 108; non-verbal IQ, 113; verbal IQ, 96
 61318543
 61365103
  46560
 hg18
 Duplication
 No
  sanders_11_ASD_discovery_cases-12233.p1
 5
 M
 Autism
 NA
 Full-scale IQ, 106; non-verbal IQ, 108; verbal IQ, 99
 63231043
 63285508
  54465
 hg18
 Duplication
 No
  sanders_11_ASD_discovery_cases-12405.p1
 6
 M
 Autism
 NA
 Full-scale IQ, 101; non-verbal IQ, 102; verbal IQ, 99
 62409842
 62763670
  353828
 hg18
 Deletion
 No
  sanders_11_ASD_discovery_cases-12997.p1
 9
 M
 Autism
 NA
 Full-scale IQ, 97; non-verbal IQ, 94; verbal IQ, 103
 63188807
 63285508
  96701
 hg18
 Deletion
 No
  prasad_12_ASD_discovery_cases-case88009
 NA
 M
 ASD
 Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. CNV identified by previous SNP microarray study
 
 63500487
 63621123
  120637
 
 Duplication
 No
  prasad_12_ASD_discovery_cases-case60984L
 NA
 M
 ASD
 Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. CNV identified by previous SNP microarray study
 
 60569383
 60672039
  102657
 
 Duplication
 No
  girirajan_13b_ASD_discovery_cases-3205102622
 N/A
 N/A
 Autism
 Diagnosis of autism confirmed by ADOS and ADI-R. Ethnicity: Hispanic
 N/A
 63213507
 63618065
  404558
 Build36/hg18
 Duplication
 No
  walker_13_ASD_discovery_cases-case1-0138-004
 N/A
 M
 ASD
 N/A
 N/A
 60567730
 60676136
  108406
 hg18
 Duplication
 No
  sajan_13_ACC/CBLH/PMG_discovery_cases-case1004-0
 N/A
 N/A
 ACC
 Diagnosis of agenesis of the corpus callosum (ACC). ASD: unknown. Seizures: unknown.
 Developmental delay: unknown. Intellectual disability: yes.
 63158774
 63271229
  112456
 hg18
 Deletion
 No
  sajan_13_ACC/CBLH/PMG_discovery_cases-case1083-0
 N/A
 N/A
 ACC
 Diagnosis of agenesis of the corpus callosum (ACC). ASD: no. Seizures: no.
 Developmental delay: yes. Intellectual disability: no.
 63158774
 63244537
  85764
 hg18
 Deletion
 No
  sajan_13_ACC/CBLH/PMG_discovery_cases-case1200-0
 N/A
 N/A
 ACC
 Diagnosis of agenesis of the corpus callosum (ACC). ASD: no. Seizures: no.
 Developmental delay: yes. Intellectual disability: unknown.
 63168260
 63310840
  142581
 hg18
 Duplication
 No
  sajan_13_ACC/CBLH/PMG_discovery_cases-case1022-0
 N/A
 N/A
 ACC-CBLH
 Diagnosis of agenesis of the corpus callosum (ACC) and cerebellar hypoplasia (CBLH). ASD: no. Seizures: yes.
 Developmental delay: yes. Intellectual disability: no.
 63231043
 63310840
  79798
 hg18
 Duplication
 No
  sajan_13_ACC/CBLH/PMG_discovery_cases-caseLR08-114
 N/A
 N/A
 CBLH
 Diagnosis of cerebellar hypoplasia (CBLH).
 
 63158774
 63244537
  85764
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case14113_2030
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63157485
 63271229
  113744
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case14128_2240
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63188981
 63277373
  88392
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case14236_2610
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63196854
 63277373
  80519
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case3009_4
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63200077
 63277373
  77296
 hg18
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case4219_1
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63325775
 63834244
  508469
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case4529_1
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 61318543
 61393758
  75215
 hg18
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case4541_1
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63157485
 63271229
  113744
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case4549_1
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 61318543
 61400167
  81624
 hg18
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case5029_4
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63157485
 63268659
  111174
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case5039_4
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 60567730
 60676136
  108406
 hg18
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case5213_3
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63500894
 63622987
  122093
 hg18
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case5325_3
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63157485
 63271229
  113744
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case5402_3
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63208758
 63277373
  68615
 hg18
 Duplication
 No
  engchuan_15_ASD_discovery_cases-case8452_201
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 63157485
 63271229
  113744
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case8497_202
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 61666580
 61766720
  100140
 hg18
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case8629_201
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 61996997
 62045071
  48074
 hg18
 Duplication
 No
  mosca_16_DCD_discovery_cases-case107803
 N/A
 M
 DCD (with or without ADHD and/or RD)
 Ancestry: unknown. Family history: maternal diagnosis unknown; paternal diagnosis unknown.
 
 65409884
 65468029
  58146
 GRCh37/hg19
 Duplication
 No
  mosca_16_DCD_discovery_cases-case112903
 N/A
 M
 DCD (with or without ADHD and/or RD)
 Ancestry: unknown. Family history: maternal diagnosis unknown; paternal diagnosis unknown.
 
 64172729
 64310757
  138029
 GRCh37/hg19
 Duplication
 No
  leppa_16_ASD_discovery_cases-AU2679301
 N/A
 M
 ASD
 
 
 64304000
 64881000
  700000
 GRCh37/hg19
 Duplication
 No

Controls

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  sanders_11_ASD_discovery_controls-11048.s1
  8
  M
  Control (matched sibling)
  NA
  NA
  63115695
  63357882
  242187
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-11121.s1
  16
  F
  Control (matched sibling)
  NA
  NA
  62104068
  62185707
  81639
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-11345.s1
  8
  M
  Control (matched sibling)
  NA
  NA
  62794273
  63001477
  207204
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-11415.s1
  13
  M
  Control (matched sibling)
  NA
  NA
  63231043
  63277373
  46330
  hg18
  Duplication
  No
  sanders_11_ASD_discovery_controls-11519.s1
  4
  F
  Control (matched sibling)
  NA
  NA
  62989519
  63310840
  321321
  hg18
  Duplication
  No
  sanders_11_ASD_discovery_controls-11521.s1
  15
  F
  Control (matched sibling)
  NA
  NA
  63157485
  63276677
  119192
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-11808.s1
  12
  F
  Control (matched sibling)
  NA
  NA
  63157485
  63271229
  113744
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-11831.s1
  7
  F
  Control (matched sibling)
  NA
  NA
  63231043
  63246760
  15717
  hg18
  Duplication
  No
  sanders_11_ASD_discovery_controls-11940.s1
  6
  M
  Control (matched sibling)
  NA
  NA
  61996997
  62019754
  22757
  hg18
  Duplication
  No
  sanders_11_ASD_discovery_controls-11941.s1
  8
  F
  Control (matched sibling)
  NA
  NA
  64054018
  64058147
  4129
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-12106.s1
  10
  F
  Control (matched sibling)
  NA
  NA
  63157485
  63268659
  111174
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-12206.s1
  13
  M
  Control (matched sibling)
  NA
  NA
  62979204
  63020620
  41416
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-12233.s1
  6
  F
  Control (matched sibling)
  NA
  NA
  63221291
  63268659
  47368
  hg18
  Duplication
  No
  sanders_11_ASD_discovery_controls-12645.s1
  11
  M
  Control (matched sibling)
  NA
  NA
  61331282
  61648231
  316949
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-12784.s1
  8
  M
  Control (matched sibling)
  NA
  NA
  62001427
  62127880
  126453
  hg18
  Duplication
  No
  sanders_11_ASD_discovery_controls-12901.s1
  4
  M
  Control (matched sibling)
  NA
  NA
  64080366
  64094066
  13700
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-12997.s1
  5
  F
  Control (matched sibling)
  NA
  NA
  63188981
  63277373
  88392
  hg18
  Deletion
  No
  sanders_11_ASD_discovery_controls-13051.s1
  9
  F
  Control (matched sibling)
  NA
  NA
  61087461
  61090632
  3171
  hg18
  Deletion
  No
  levy_11_ASD_discovery_controls-11519.s1
  NA
  F
  Control
  NA
  NA
  62990868
  63305416
  314549
  hg18
  Duplication
  No
  engchuan_15_ASD_discovery_controls-controlHABC_902951_902951
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63271229
  113744
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_902888_902888
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63263682
  106197
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_902884_902884
  N/A
  N/A
  Control
  No previous psychiatric history
 
  62414499
  62451877
  37378
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_902688_902688
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63221291
  63277373
  56082
  hg18
  Duplication
  No
  engchuan_15_ASD_discovery_controls-controlHABC_902674_902674
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63271229
  113744
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_901081_901081
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63271229
  113744
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_901042_901042
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63310840
  63834522
  523682
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_901027_901027
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63268659
  111174
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_900621_900621
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63271229
  113744
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_900605_900605
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63196854
  63276677
  79823
  hg18
  Duplication
  No
  engchuan_15_ASD_discovery_controls-controlHABC_900576_900576
  N/A
  N/A
  Control
  No previous psychiatric history
 
  62104068
  62161921
  57853
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_900515_900515
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63268659
  111174
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlHABC_900478_900478
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63268659
  111174
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlB929351_1007853649
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63221291
  63277373
  56082
  hg18
  Duplication
  No
  engchuan_15_ASD_discovery_controls-controlB791125_1007873652
  N/A
  N/A
  Control
  No previous psychiatric history
 
  62219873
  62527158
  307285
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlB782197_1007875255
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63277373
  119888
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlB595540_1007848526
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63444758
  63616854
  172096
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlB543816_1007853746
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63196854
  63310840
  113986
  hg18
  Duplication
  No
  engchuan_15_ASD_discovery_controls-controlB505778_1007874875
  N/A
  N/A
  Control
  No previous psychiatric history
 
  63157485
  63271229
  113744
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlB238990_1007852925
  N/A
  N/A
  Control
  No previous psychiatric history
 
  62569077
  62612850
  43773
  hg18
  Deletion
  No
  engchuan_15_ASD_discovery_controls-controlB191955_1007874255
  N/A
  N/A
  Control
  No previous psychiatric history
 
  62115956
  62305059
  189103
  hg18
  Duplication
  No
  engchuan_15_ASD_discovery_controls-control110036014843_
  N/A
  N/A
  Control
  No previous psychiatric history
 
  61337787
  61386776
  48989
  hg18
  Duplication
  No
  kanduri_15_ASD_discovery_controls-control_split1532
  N/A
  N/A
  Control
  Control screened for DSM-IV mental disorders using the Composite International Diagnostic Interview and psychotic disorders using the research version of the Structured Clinical Interview for DSM-IV
 
  65432790
  65549877
  117088
  N/A
  Deletion
  No

Cases

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
 marshall_08_ASD_discovery_cases-NA0028-000
 qPCR, qmPCR
 
 Unknown
 NA
 NA
 0 genes
 
 pinto_10_ASD_discovery_cases-case13094_1113
 qPCR
 
 De novo
 NA
 NA
 OR7E156P
 
 pinto_10_ASD_discovery_cases-case5029_4
 Agilent1M
 
 paternal
 NA
 NA
 OR7E156P
 
 pinto_10_ASD_discovery_cases-case5039_4
 Agilent1M
 
 maternal
 NA
 NA
 0 genes
 
 pinto_10_ASD_discovery_cases-case5213_3
 Agilent1M
 
 maternal
 NA
 NA
 0 genes
 
 pinto_10_ASD_discovery_cases-case5325_3
 Agilent1M
 
 maternal
 NA
 NA
 OR7E156P
 
 gai_11_ASD_discovery_cases-AU1590302
 
 
 Inherited
 
 
 0 genes
 
 gai_11_ASD_replication_cases-AU070004
 
 
 Inherited
 
 
 0 genes
 
 gai_11_ASD_replication_cases-AU070005
 
 
 Inherited
 
 
 0 genes
 
 gai_11_ASD_replication_cases-AU070008
 
 
 Inherited
 
 
 0 genes
 
 gai_11_ASD_replication_cases-AU071703
 
 
 Inherited
 
 
 0 genes
 
 gai_11_ASD_replication_cases-AU075503
 
 
 Inherited
 
 
 0 genes
 
 gai_11_ASD_replication_cases-AU083103
 
 
 Inherited
 
 
 0 genes
 
 nord_11_ASD_discovery_cases-206-1
 
 
 Maternal
 
 
 0 genes
 
 sanders_11_ASD_discovery_cases-11027.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Segregated
 0 genes
 
 sanders_11_ASD_discovery_cases-11121.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Segregated
 0 genes
 
 sanders_11_ASD_discovery_cases-11145.p1
 
 
 Unknown
 Simplex (trio)
 NA
 0 genes
 
 sanders_11_ASD_discovery_cases-11316.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Segregated
 0 genes
 
 sanders_11_ASD_discovery_cases-11327.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 0 genes
 
 sanders_11_ASD_discovery_cases-11398.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Not segregated
 0 genes
 
 sanders_11_ASD_discovery_cases-11521.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Not segregated
 OR7E156P
 
 sanders_11_ASD_discovery_cases-11808.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Not segregated
 OR7E156P
 
 sanders_11_ASD_discovery_cases-11940.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Not segregated
 0 genes
 
 sanders_11_ASD_discovery_cases-12215.p1
 
 
 Maternal
 Simplex (trio)
 NA
 0 genes
 
 sanders_11_ASD_discovery_cases-12233.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 0 genes
 
 sanders_11_ASD_discovery_cases-12405.p1
 
 
 Maternal
 Simplex (trio)
 NA
 0 genes
 
 sanders_11_ASD_discovery_cases-12997.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Not segregated
 OR7E156P
 
 prasad_12_ASD_discovery_cases-case88009
 
 
 Unknown
 Unknown
 Unknown
 0 genes
 
 prasad_12_ASD_discovery_cases-case60984L
 
 
 Unknown
 Unknown
 Unknown
 MIR3169
 
 girirajan_13b_ASD_discovery_cases-3205102622
 
 
 Unknown
 Unknown
 Unknown
 0 genes
 
 walker_13_ASD_discovery_cases-case1-0138-004
 
 
 Unknown
 Multiplex
 Unknown
 0 genes
 
 sajan_13_ACC/CBLH/PMG_discovery_cases-case1004-0
 Not tested by qPCR
 
 Unknown
 Unknown
 Unknown
 OR7E156P
 
 sajan_13_ACC/CBLH/PMG_discovery_cases-case1083-0
 Not tested by qPCR
 
 Unknown
 Unknown
 Unknown
 OR7E156P
 
 sajan_13_ACC/CBLH/PMG_discovery_cases-case1200-0
 Not tested by qPCR
 
 Unknown
 Unknown
 Unknown
 AK098560,AK127969,OR7E156P
 
 sajan_13_ACC/CBLH/PMG_discovery_cases-case1022-0
 Not tested by qPCR
 
 Unknown
 Unknown
 Unknown
 AK098560,AK127969
 
 sajan_13_ACC/CBLH/PMG_discovery_cases-caseLR08-114
 Not tested by qPCR
 
 Unknown
 Unknown
 Unknown
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case14113_2030
 
 
 Unknown
 
 
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case14128_2240
 
 
 Unknown
 
 
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case14236_2610
 
 
 Unknown
 
 
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case3009_4
 
 
 Unknown
 
 
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case4219_1
 
 
 Unknown
 
 
 0 genes
 
 engchuan_15_ASD_discovery_cases-case4529_1
 
 
 Unknown
 
 
 0 genes
 
 engchuan_15_ASD_discovery_cases-case4541_1
 
 
 Unknown
 
 
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case4549_1
 
 
 Unknown
 
 
 0 genes
 
 engchuan_15_ASD_discovery_cases-case5029_4
 
 
 Unknown
 
 
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case5039_4
 
 
 Unknown
 
 
 MIR3169
 
 engchuan_15_ASD_discovery_cases-case5213_3
 
 
 Unknown
 
 
 0 genes
 
 engchuan_15_ASD_discovery_cases-case5325_3
 
 
 Unknown
 
 
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case5402_3
 
 
 Unknown
 
 
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case8452_201
 
 
 Unknown
 
 
 OR7E156P
 
 engchuan_15_ASD_discovery_cases-case8497_202
 
 
 Unknown
 
 
 0 genes
 
 engchuan_15_ASD_discovery_cases-case8629_201
 
 
 Unknown
 
 
 0 genes
 
 mosca_16_DCD_discovery_cases-case107803
 
 
 Unknown
 Unknown
 Unknown
 0 RefSeq genes
 
 mosca_16_DCD_discovery_cases-case112903
 
 
 Unknown
 Unknown
 Unknown
 0 RefSeq genes
 
 leppa_16_ASD_discovery_cases-AU2679301
 
 
 Paternal
 Simplex
 Unknown
 LINC00395, OR7E156P
 

Controls

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
sanders_11_ASD_discovery_controls-11048.s1
 
 
  Maternal
  Simplex (quad)
  NA
  OR7E156P
 
sanders_11_ASD_discovery_controls-11121.s1
 
 
  Both parents
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-11345.s1
 
 
  Unknown
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-11415.s1
 
 
  Maternal
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-11519.s1
 
 
  Paternal
  Simplex (quad)
  NA
  OR7E156P
 
sanders_11_ASD_discovery_controls-11521.s1
 
 
  Maternal
  Simplex (quad)
  NA
  OR7E156P
 
sanders_11_ASD_discovery_controls-11808.s1
 
 
  Maternal
  Simplex (quad)
  NA
  OR7E156P
 
sanders_11_ASD_discovery_controls-11831.s1
 
 
  Paternal
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-11940.s1
 
 
  Maternal
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-11941.s1
 
 
  Unknown
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-12106.s1
 
 
  Maternal
  Simplex (quad)
  NA
  OR7E156P
 
sanders_11_ASD_discovery_controls-12206.s1
 
 
  Maternal
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-12233.s1
 
 
  Paternal
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-12645.s1
 
 
  Paternal
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-12784.s1
 
 
  Paternal
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-12901.s1
 
 
  Maternal
  Simplex (quad)
  NA
  0 genes
 
sanders_11_ASD_discovery_controls-12997.s1
 
 
  Maternal
  Simplex (quad)
  NA
  OR7E156P
 
sanders_11_ASD_discovery_controls-13051.s1
 
 
  Paternal
  Simplex (quad)
  NA
  0 genes
 
levy_11_ASD_discovery_controls-11519.s1
 
 
  Paternal
  Simplex
  NA
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlHABC_902951_902951
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlHABC_902888_902888
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlHABC_902884_902884
 
 
  Unknown
 
 
  0 genes
 
engchuan_15_ASD_discovery_controls-controlHABC_902688_902688
 
 
  Unknown
 
 
  0 genes
 
engchuan_15_ASD_discovery_controls-controlHABC_902674_902674
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlHABC_901081_901081
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlHABC_901042_901042
 
 
  Unknown
 
 
  0 genes
 
engchuan_15_ASD_discovery_controls-controlHABC_901027_901027
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlHABC_900621_900621
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlHABC_900605_900605
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlHABC_900576_900576
 
 
  Unknown
 
 
  0 genes
 
engchuan_15_ASD_discovery_controls-controlHABC_900515_900515
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlHABC_900478_900478
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlB929351_1007853649
 
 
  Unknown
 
 
  0 genes
 
engchuan_15_ASD_discovery_controls-controlB791125_1007873652
 
 
  Unknown
 
 
  0 genes
 
engchuan_15_ASD_discovery_controls-controlB782197_1007875255
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlB595540_1007848526
 
 
  Unknown
 
 
  0 genes
 
engchuan_15_ASD_discovery_controls-controlB543816_1007853746
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlB505778_1007874875
 
 
  Unknown
 
 
  OR7E156P
 
engchuan_15_ASD_discovery_controls-controlB238990_1007852925
 
 
  Unknown
 
 
  0 genes
 
engchuan_15_ASD_discovery_controls-controlB191955_1007874255
 
 
  Unknown
 
 
  0 genes
 
engchuan_15_ASD_discovery_controls-control110036014843_
 
 
  Unknown
 
 
  0 genes
 
kanduri_15_ASD_discovery_controls-control_split1532
 
 
  Unknown
 
 
  Intergenic CNV: nearest genes, OR7E156P(dist=1116089),PCDH9(dist=1327089)
 

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