12p12.2CNV Type: Deletion-Duplication
Largest CNV size: 107993 bp
Statistics Box:
Number of Reports: 10
Number of Reports: 10
Summary Information
Summary statement in development
Additional Locus Information
References
Major Reports
Title
Author, Year
Report Class
CNV Type
Functional impact of global rare copy number variation in autism spectrum disorders.
Deletion
Excess of rare, inherited truncating mutations in autism.
Deletion-Duplication
Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder
Deletion
Minor Reports
Title
Author, Year
Report Class
CNV Type
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Deletion-Duplication
Rare de novo and transmitted copy-number variation in autistic spectrum disorders.
Deletion
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.
Deletion
Performance of case-control rare copy number variation annotation in classification of autism.
Deletion
Cases
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
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
34261
2
0
2
han_22_ASD/DD/ID_discovery_cases
Probands with ASD or unexplained developmental delay/intellectual disability with or without other congenital anomalies from Shandong province in Northern China who were referred for genetic services from January 2014 to December 2018.
410
151 cases diagnosed with ASD (DSM-5 criteria, ADOS-2, confirmed by CARS score > 30) and 259 patients diagnosed with developmental delay/intellectual disability (DSM-5 criteria, confirmed by Gesell developmental scale DQ score < 75 and Wechsler Intelligence Scale for Children-Revised with IQ<70).
Mean age, 2 yrs. 11 mos.
68.78% Male
41772
0
1
1
krumm_15_ASD_discovery_cases
Probands from the Simons Simplex Collection
2377
Diagnosis of ASD
N/A
N/A
65148
7
1
8
kushima_22_SCZ_discovery_cases
Japanese schizophrenia probands evaluated for copy number variation from an initial cohort of 3,111 probands before quality control.
3014
Cases diagnosed with schizophrenia (SCZ) according to DSM-5 criteria.
Median age, 45 yrs.
53.5% Male
20338
1
0
1
larson_17_ASD_discovery_cases
Participants with a dual diagnosis of ASD and psychosis that were recruited from clinical services in the public and independent sectors in the United Kingdom, as well as from charities and an Asperger's syndrome social networking website (study took place from January 2011 and April 2014)
116
All cases with a dual diagnosis of ASD and psychosis (affective, schizophrenic, and atypical)
N/A
N/A
24010
0
1
1
levy_11_ASD_discovery_cases
Autistic probands from 887 families from the Simons Simplex Collection (SSC)
858
ASD
87.06% Male
106993
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
32405
1
0
1
poultney_13_ASD_discovery_cases
ASD cases of European ancestry from AGRE retained after filtering (original cohort size of 432 cases)
299
Cases diagnosed with ASD
N/A
79.86% Male (before filtering)
8372
1
0
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
107993
9
1
10
stamouli_18_ASD/NDD_discovery_cases
Affected individuals from 100 twin pairs (69 monozygotic, 31 dizygotic), corresponding to 97 families, that were enriched for neurodevelopmental disorders from the Roots of Autism and ADHD Study in Sweden (RATSS)
100 twin pairs
Diagnoses based on DSM-5 criteria following evaluation using standard diagnostic tools [a psychosocial and anamnestic interview, the Autism Diagnosis Interview-Revised (ADI-R), the Autism Diagnostic Observation Schedule Second Edition (ADOS-2), the Kiddie Schedule for Affective Disorders and Schizophrenia (K-SADS), or the Diagnostic Interview for ADHD in Adults (DIVA)]; Wechsler Intelligence Scale for Children or Adults, Fourth Edition (WISC-IV) or the Leiter-revised scales in combination with the Peabody Picture Vocabulary Test, Third Edition, and the parent-based Adaptive Behavior Assessment Scale, 2nd Edition (ABAS-2) were also used to evaluate adaptive, cognitive, and verbal abilities an
N/A
N/A
120278
2
0
2
Controls
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
bacchelli_20_ASD_discovery_controls
Anonymized DNA samples from Italian individuals with no psychiatric disorders
365
Control
N/A
54.52% Male
11695
1
0
1
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
67376
1
1
2
krumm_15_ASD_discovery_controls
Unaffected siblings from quad families from the Simons Simplex Collection
1786
Control
N/A
N/A
61222
5
1
6
kushima_22_ASD/BPD/SCZ_discovery_controls
Psychiatrically normal control individuals selected from the general population evaluated for copy number variation from an initial cohort of 2,713 control individuals before quality control.
2671
Controls were psychiatrically normal and had no history of mental disorders based on responses to questionnaires or self-reporting.
Median age, 36 yrs.
47.8% Male
0
0
0
0
larson_17_ASD_discovery_controls
Entries listed in the Database of Genomic Variants (up to October 2017)
N/A
Control
N/A
N/A
24010
0
1
1
levy_11_ASD_discovery_controls
Unaffected siblings of autistic probands from 887 families from the Simons Simplex Collection (SSC)
863
Control
47.97% Male
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.
46434
1
0
1
poultney_13_ASD_discovery_controls
Controls matched for European ancestry from NIMH and CEPH retained after filtering (original cohort size of 379 controls)
260
Control
N/A
47.49% Male (before filtering)
20851
2
0
2
sanders_11_ASD_discovery_controls
Matched siblings of autistic probands from the Simons Simplex Collection (SSC).
872
Controls
Mean, 10.0 yrs.
408695
5
0
5
Cases
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
engchuan_15_ASD_discovery_cases
Caucasian
Solid phase hybridization
Illumina 1M
None
han_22_ASD/DD/ID_discovery_cases
Han Chinese
Array SNP
Affymetrix SNP 6.0, Affymetrix CytoScan HD
krumm_15_ASD_discovery_cases
N/A
WES
CoNIFER, XHMM
Solid phase hybridization (Illumina 1M, 1 M Duo, or Omni 2.5)
kushima_22_SCZ_discovery_cases
Japan
aCGH
NimbleGen 720K Whole-Genome Tiling, Agilent SurePrint G3 Human CGH 400K
Fast Adaptive States Segmentation Technique 2
BioDiscovery Nexus Copy Number v.9.0
qRT-PCR
larson_17_ASD_discovery_cases
United Kingdom
Array SNP
Affymetrix CytoScan HD 2.8M, Affymetrix Cytogenetics
SNP-FASST2 Segmentation
Nexus Copy Number 7 (BioDiscovery), Affymetrix ChAS
None
levy_11_ASD_discovery_cases
aCGH
NimbleGen HD2
HMM
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), array SNP (Affymetrix 500K)
poultney_13_ASD_discovery_cases
European
WES
Agilent SureSelect Human All Exon v.2
XHMM
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, Illumina 1M v3
PennCNV, QuantiSNP, GNOSIS
stamouli_18_ASD/NDD_discovery_cases
Swedish
Solid phase hybridization
Illumina Infinium PsychArray-24 v1.1
PennCNV, QuantiSNP, iPattern, iPsychCNV
None
Controls
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
bacchelli_20_ASD_discovery_controls
Italian
Solid phase hybridization
Illumina Infinium PsychArray
PennCNV, QuantiSNP, CNVPartition
None
engchuan_15_ASD_discovery_controls
Caucasian
Solid phase hybridization
Illumina 1M
None
krumm_15_ASD_discovery_controls
N/A
WES
CoNIFER, XHMM
Solid phase hybridization (Illumina 1M, 1 M Duo, or Omni 2.5)
kushima_22_ASD/BPD/SCZ_discovery_controls
Japan
aCGH
NimbleGen 720K Whole-Genome Tiling, Agilent SurePrint G3 Human CGH 400K
Fast Adaptive States Segmentation Technique 2
BioDiscovery Nexus Copy Number v.9.0
qRT-PCR
larson_17_ASD_discovery_controls
N/A
N/A
N/A
levy_11_ASD_discovery_controls
aCGH
NimbleGen HD2
HMM
nord_11_ASD_discovery_controls
aCGH
NimbleGen HD2
Sliding-window algorithm, ~10 kb minumum size threshold
None
poultney_13_ASD_discovery_controls
European
WES
Agilent SureSelect Human All Exon v.2
XHMM
None
sanders_11_ASD_discovery_controls
Solid phase hybridization
Illumina 1M v1 or Illumina 1M v3
PennCNV, QuantiSNP, GNOSIS
Cases
Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
engchuan_15_ASD_discovery_cases-case13046_553
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
20571418
20605679
34262
GRCh38
Deletion
No
engchuan_15_ASD_discovery_cases-case5112_4
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
20888700
20921104
32405
GRCh38
Deletion
No
han_22_ASD/DD/ID_discovery_cases-caseY108
4 yrs. 7 mos.
M
ASD
20845153
20886924
41772
GRCh38
Duplication
No
krumm_15_ASD_discovery_cases-case11285.p1
N/A
Male
ASD
Proband from the Simons Simplex Collection (SSC). Family type: Quad
20862755
20883604
20850
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_cases-case11329.p1
N/A
Male
ASD
Proband from the Simons Simplex Collection (SSC). Family type: Trio
20875234
20883604
8371
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_cases-case12382.p1
N/A
Male
ASD
Proband from the Simons Simplex Collection (SSC). Family type: Quad
20750674
20815822
65149
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_cases-case12655.p1
N/A
Male
ASD
Proband from the Simons Simplex Collection (SSC). Family type: Quad
20875234
20883604
8371
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_cases-case13134.p1
N/A
Male
ASD
Proband from the Simons Simplex Collection (SSC). Family type: Trio
20875234
20883602
8369
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_cases-case13864.p1
N/A
Male
ASD
Proband from the Simons Simplex Collection (SSC). Family type: Quad
20858438
20862856
4419
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_cases-case14181.p1
N/A
Male
ASD
Proband from the Simons Simplex Collection (SSC). Family type: Quad
20855027
20916249
61223
GRCh38
Duplication
Yes
krumm_15_ASD_discovery_cases-case14272.p1
N/A
Male
ASD
Proband from the Simons Simplex Collection (SSC). Family type: Quad
20875234
20883604
8371
GRCh38
Deletion
Yes
kushima_22_SCZ_discovery_cases-caseSCZ2385
NA
NA
Schizophrenia
Diagnosis of schizophrenia according to DSM-5 criteria.
20857217
20877554
20338
GRCh38
Deletion
Yes
larson_17_ASD_discovery_cases-case86
N/A
N/A
ASD and psychosis
No additional clinical information available. Patient carries CNV that is present in DGV (less than 1.5%) but was not present in 1124 ASD cases without psychosis from the Simons Simplex Collection.
20417636
20441646
24011
GRCh38
Duplication
No
levy_11_ASD_discovery_cases-12382.p1
NA
M
ASD
NA
NA
20746569
20853561
106993
GRCh38
Deletion
No
pinto_10_ASD_discovery_cases-case5112_4
NA
M
ASD
NA
NA
20888700
20921104
32405
GRCh38
Deletion
Yes
poultney_13_ASD_discovery_cases-case98HI0371B
N/A
M
ASD
ASD case from AGRE (AGRE ID AU032804; NDAR ID N/A)
20875233
20883604
8372
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11107.p1
6.9
M
Autism
NA
Full-scale IQ, 30; non-verbal IQ, 37; verbal IQ, 25
20915248
20929342
14095
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11285.p1
15.3
M
Autism
NA
Full-scale IQ, 13; non-verbal IQ, 20; verbal IQ, 5
20865197
20886215
21019
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11329.p1
8.7
M
Autism
NA
Full-scale IQ, 104; non-verbal IQ, 105; verbal IQ, 103
20865197
20883599
18403
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11370.p1
14.6
M
Autism
NA
Full-scale IQ, 100; non-verbal IQ, 110; verbal IQ 102
20434258
20501634
67377
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-11391.p1
15.2
M
Autism
NA
Full-scale IQ, 116; non-verbal IQ, 116; verbal IQ, 113
20862205
20883599
21395
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11556.p1
9.7
M
Autism
NA
Full-scale IQ, 102; non-verbal IQ, 102; verbal IQ, 108
20184251
20186007
1757
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12382.p1
10.1
M
Autism
NA
Full-scale IQ, 91; non-verbal IQ, 94; verbal IQ, 88
20745188
20853181
107994
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12382.p1
10.1
M
Autism
NA
Full-scale IQ, 91; non-verbal IQ, 94; verbal IQ, 88
20728828
20734057
5230
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12449.p1
6.8
M
Autism
NA
Full-scale IQ, 87; non-verbal IQ, 87; verbal IQ, 93
20184251
20186007
1757
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12655.p1
8.9
M
Autism
NA
Full-scale IQ, 48; non-verbal IQ, 64; verbal IQ, 28
20864354
20883599
19246
GRCh38
Deletion
No
stamouli_18_ASD/NDD_discovery_cases-family5_Twin_1
N/A
N/A
ASD/NDD
Case is from a monozygotic twin pair from the Discordant ASD/Concordant NDD diagnostic group
20732904
20853181
120278
GRCh38
Deletion
No
stamouli_18_ASD/NDD_discovery_cases-family5_Twin_2
N/A
N/A
ASD/NDD
Case is from a monozygotic twin pair from the Discordant ASD/Concordant NDD diagnostic group
20732904
20853181
120278
GRCh38
Deletion
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
bacchelli_20_ASD_discovery_controls-control20054
N/A
F
Control
Control
20871905
20883599
11695
GRCh38
Deletion
No
engchuan_15_ASD_discovery_controls-control110036015782_
N/A
N/A
Control
No previous psychiatric history
20434258
20501634
67377
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB850068_1007871741
N/A
N/A
Control
No previous psychiatric history
20888700
20921104
32405
GRCh38
Deletion
No
krumm_15_ASD_discovery_controls-control11285.s1
N/A
Male
Control
Unaffected sibling from the Simons Simplex Collection (SSC)
20875234
20883604
8371
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_controls-control13072.s1
N/A
Female
Control
Unaffected sibling from the Simons Simplex Collection (SSC)
20875234
20883604
8371
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_controls-control13129.s1
N/A
Female
Control
Unaffected sibling from the Simons Simplex Collection (SSC)
20875234
20883604
8371
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_controls-control13855.s1
N/A
Female
Control
Unaffected sibling from the Simons Simplex Collection (SSC)
20875234
20883604
8371
GRCh38
Deletion
Yes
krumm_15_ASD_discovery_controls-control14181.s1
N/A
Female
Control
Unaffected sibling from the Simons Simplex Collection (SSC)
20855027
20916249
61223
GRCh38
Duplication
Yes
krumm_15_ASD_discovery_controls-control14272.s1
N/A
Female
Control
Unaffected sibling from the Simons Simplex Collection (SSC)
20875234
20883604
8371
GRCh38
Deletion
Yes
nord_11_ASD_discovery_controls-04C27935
Control
19958300
20004733
46434
Unknown
Deletion
poultney_13_ASD_discovery_controls-control04C27734A
N/A
F
Control
NIMH Control (NIMH ID 28812)
20862754
20883604
20851
GRCh38
Deletion
No
poultney_13_ASD_discovery_controls-control04C31231A
N/A
M
Control
NIMH Control (NIMH ID 33455)
20875233
20883604
8372
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-11107.s1
3.7
M
Control (matched sibling)
NA
NA
20915248
20933449
18202
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-11285.s1
16.4
M
Control (matched sibling)
NA
NA
20865197
20883599
18403
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-11329.s1
6.9
M
Control (matched sibling)
NA
NA
20862676
20883599
20924
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-11753.s1
15.1
F
Control (matched sibling)
NA
NA
20864354
20884619
20266
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-13072.s1
8.7
F
Control (matched sibling)
NA
NA
20864354
20883599
19246
GRCh38
Deletion
No
Cases
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
engchuan_15_ASD_discovery_cases-case13046_553
Unknown
PDE3A
engchuan_15_ASD_discovery_cases-case5112_4
Unknown
SLCO1B3
han_22_ASD/DD/ID_discovery_cases-caseY108
Unknown
SLCO1B3,SLCO1B3-SLCO1B7
krumm_15_ASD_discovery_cases-case11285.p1
Illumina 1M
Paternal
Simplex
Not segregated (CNV in unaffected sibling)
SLCO1B3
krumm_15_ASD_discovery_cases-case11329.p1
Illumina 1M
Maternal
Simplex
Segregated
SLCO1B3
krumm_15_ASD_discovery_cases-case12382.p1
Illumina 1MDuo
Paternal
Simplex
Segregated
SLCO1C1,SLCO1B3
krumm_15_ASD_discovery_cases-case12655.p1
Illumina 1MDuo
Paternal
Simplex
Segregated
SLCO1B3
krumm_15_ASD_discovery_cases-case13134.p1
1M-Duov3
Paternal
Simplex
Segregated
SLCO1B3
krumm_15_ASD_discovery_cases-case13864.p1
Omni2.5-4v1
Paternal
Simplex
Segregated
SLCO1B3
krumm_15_ASD_discovery_cases-case14181.p1
Omni2.5-4v1
Maternal
Simplex
Not segregated (CNV in unaffected sibling)
SLCO1B3
krumm_15_ASD_discovery_cases-case14272.p1
Omni2.5-4v1
Paternal
Simplex
Not segregated (CNV in unaffected sibling)
SLCO1B3
kushima_22_SCZ_discovery_cases-caseSCZ2385
qRT-PCR
Unknown
SLCO1B3,SLCO1B3-SLCO1B7
larson_17_ASD_discovery_cases-case86
Unknown
Unknown
PDE3A
levy_11_ASD_discovery_cases-12382.p1
Paternal
Simplex
Segregated
SLCO1C1,SLCO1B3
pinto_10_ASD_discovery_cases-case5112_4
Agilent1M
paternal
NA
NA
SLCO1B3
poultney_13_ASD_discovery_cases-case98HI0371B
Unknown
Unknown (likely multiplex/AGRE)
Unknown
SLCO1B3
sanders_11_ASD_discovery_cases-11107.p1
Paternal
Simplex (quad-proband matched)
Not segregated
SLCO1B3
sanders_11_ASD_discovery_cases-11285.p1
Paternal
Simplex (quad-proband matched)
Not segregated
SLCO1B3
sanders_11_ASD_discovery_cases-11329.p1
Maternal
Simplex (quad-proband matched)
Not segregated
SLCO1B3
sanders_11_ASD_discovery_cases-11370.p1
Paternal
Simplex (trio)
NA
UBE2L2,PDE3A
sanders_11_ASD_discovery_cases-11391.p1
Maternal
Simplex (quad-proband matched)
Not segregated
SLCO1B3
sanders_11_ASD_discovery_cases-11556.p1
Maternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-12382.p1
Paternal
Simplex (quad-proband matched)
Not segregated
SLCO1C1,SLCO1B3
sanders_11_ASD_discovery_cases-12382.p1
Paternal
Simplex (quad-proband matched)
Not segregated
SLCO1C1
sanders_11_ASD_discovery_cases-12449.p1
Paternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-12655.p1
Paternal
Simplex (quad-proband matched)
Not segregated
SLCO1B3
stamouli_18_ASD/NDD_discovery_cases-family5_Twin_1
Unknown
Multiplex
Segregated (CNV present in both affected twins)
SLCO1C1,SLCO1B3
stamouli_18_ASD/NDD_discovery_cases-family5_Twin_2
Unknown
Multiplex
Segregated (CNV present in both affected twins)
SLCO1C1,SLCO1B3
Controls
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
bacchelli_20_ASD_discovery_controls-control20054
Unknown
SLCO1B3,SLCO1B3-SLCO1B7
engchuan_15_ASD_discovery_controls-control110036015782_
Unknown
UBE2L2,PDE3A
engchuan_15_ASD_discovery_controls-controlB850068_1007871741
Unknown
SLCO1B3
krumm_15_ASD_discovery_controls-control11285.s1
Illumina 1M
Paternal
SLCO1B3
krumm_15_ASD_discovery_controls-control13072.s1
Illumina 1MDuo
Paternal
SLCO1B3
krumm_15_ASD_discovery_controls-control13129.s1
1M-Duov3
Maternal
SLCO1B3
krumm_15_ASD_discovery_controls-control13855.s1
Omni2.5-4v1
Maternal
SLCO1B3
krumm_15_ASD_discovery_controls-control14181.s1
Omni2.5-4v1
Maternal
SLCO1B3
krumm_15_ASD_discovery_controls-control14272.s1
Omni2.5-4v1
Paternal
SLCO1B3
nord_11_ASD_discovery_controls-04C27935
0 genes
poultney_13_ASD_discovery_controls-control04C27734A
Unknown
SLCO1B3
poultney_13_ASD_discovery_controls-control04C31231A
Unknown
SLCO1B3
sanders_11_ASD_discovery_controls-11107.s1
Paternal
Simplex (quad)
NA
SLCO1B3
sanders_11_ASD_discovery_controls-11285.s1
Paternal
Simplex (quad)
NA
SLCO1B3
sanders_11_ASD_discovery_controls-11329.s1
Maternal
Simplex (quad)
NA
SLCO1B3
sanders_11_ASD_discovery_controls-11753.s1
Maternal
Simplex (quad)
NA
SLCO1B3
sanders_11_ASD_discovery_controls-13072.s1
Paternal
Simplex (quad)
NA
SLCO1B3
No Animal Model Data Available