9p22.2CNV Type: Deletion-Duplication
Largest CNV size: 85334 bp
Statistics Box:
Number of Reports: 7
Number of Reports: 7
Summary Information
Summary statement in development
Additional Locus Information
References
Major Reports
Title
Author, Year
Report Class
CNV Type
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Duplication
Minor Reports
Title
Author, Year
Report Class
CNV Type
Identifying autism loci and genes by tracing recent shared ancestry.
Deletion
Rare structural variation of synapse and neurotransmission genes in autism.
Deletion
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.
Deletion
Performance of case-control rare copy number variation annotation in classification of autism.
Deletion-Duplication
Cases
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
digregorio_17_DD/ID_discovery_cases
Consecutive cases examined in the Medical Genetics Unit at the "Citta della Salte e della Scienza" University Hospital (Turin, Italy) from 2008 to 2014 (cases with CNVs are present in DECIPHER database)
1015
Cases diagnosed with idiopathic developmental delay and/or intellectual disability (DD/ID)
N/A
N/A
529000
1
0
1
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
456744
3
7
10
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
42017
2
0
2
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
85335
1
0
1
morrow_08_ASD_discovery_cases
Affected individuals from 70 families (52 simplex, 18 multiplex) recruited by Homozygosity Mapping Collaborative for Autism (HMCA) used in CNV analysis. This cohort was selected from an original population of affected individuals from 104 families (79 simplex, 25 multiplex; 82.7% male); 88 of these pedigrees have cousin marriages.
94
ASD (based on DSM-IV-TR diagnoses when research scales not available in native language)
300
1
0
1
pinto_14_ASD_discovery_cases
ASD probands from simplex and multiplex families collected as part of stage 2 of the Autism Genome Project (AGP) after quality control (1,604 before QC)
1359
Cases classified according to ADOS and ADI-R
N/A
N/A
31156
0
1
1
prasad_12_ASD_discovery_cases
Unrelated ASD cases recruited from three Canadian sites (Hospital for Sick Children, McMaster University, and Memorial University of Newfoundland); the majority of cases had been previously genotyped with results published in Marshall et al., 2008 and Pinto et al., 2010. 20 cases from initial cohort of 696 were excluded from further analysis (due to CNVs > 5 Mb).
676
Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS
NA
82.84% Male
12331
2
0
2
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
85334
6
7
13
Controls
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
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
54730
4
18
22
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)
12331
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.
49922
2
8
10
Cases
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
digregorio_17_DD/ID_discovery_cases
Italian
aCGH
Agilent 60K (SurePrint G3 Human CGH Microarray 8x60K)
ADM-2
Agilent CGH Analytics software ver. 4.0.81
None
engchuan_15_ASD_discovery_cases
Caucasian
Solid phase hybridization
Illumina 1M
None
gai_11_ASD_discovery_cases
European
Solid phase hybridization
Illumina Infinium II HumanHap550 BeadChip
BeadStudio 3.0
None
gai_11_ASD_replication_cases
European
Solid phase hybridization
Illumina Infinium II HumanHap550 BeadChip
BeadStudio 3.0
None
morrow_08_ASD_discovery_cases
Arabic Middle East, Turkey, and Pakistan
Array SNP
Affymetrix 500K
BRLMM
dChip
pinto_14_ASD_discovery_cases
Predominantly European
Solid phase hybridization
Illumina 1M (v.1 and v.3)
qPCR, MLPA, long-range PCR
prasad_12_ASD_discovery_cases
Canada
aCGH
Agilent 1M
ADM-2, DNAcopy (R Bioconductor)
DNA Analytics v4.0.85 (Agilent), DNAcopy
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
Controls
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
engchuan_15_ASD_discovery_controls
Caucasian
Solid phase hybridization
Illumina 1M
None
prasad_12_ASD_discovery_controls
NA
aCGH
Agilent 1M
ADM-2, DNAcopy (R Bioconductor)
DNA Analytics v4.0.85 (Agilent), DNAcopy
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
digregorio_17_DD/ID_discovery_cases-DECIPHER_300115
N/A
M
Developmental delay/intellectual disability
16973985
17502946
528962
GRCh38
Deletion
No
engchuan_15_ASD_discovery_cases-case13056_663
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
16911668
17028237
116570
GRCh38
Deletion
No
engchuan_15_ASD_discovery_cases-case13211_2323
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
17583312
17632813
49502
GRCh38
Duplication
No
engchuan_15_ASD_discovery_cases-case14342_4560
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
17857111
18032369
175259
GRCh38
Deletion
No
engchuan_15_ASD_discovery_cases-case16090_1571122001
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
16846325
17303069
456745
GRCh38
Duplication
No
engchuan_15_ASD_discovery_cases-case20128_4016001
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
17596835
17627990
31156
GRCh38
Duplication
No
engchuan_15_ASD_discovery_cases-case20175_1679001
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
17589823
17625004
35182
GRCh38
Duplication
No
engchuan_15_ASD_discovery_cases-case2211_1
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
17583312
17633234
49923
GRCh38
Duplication
No
engchuan_15_ASD_discovery_cases-case4147_1
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
17583312
17633234
49923
GRCh38
Duplication
No
engchuan_15_ASD_discovery_cases-case4381_1
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
17578504
17631210
52707
GRCh38
Duplication
No
engchuan_15_ASD_discovery_cases-case6270_3
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
17899608
18023979
124372
GRCh38
Deletion
No
gai_11_ASD_discovery_cases-AU1099302
Autism
16911847
16953863
42017
Unknown
Deletion
No
gai_11_ASD_discovery_cases-AU1099303
Autism
16911847
16953863
42017
Unknown
Deletion
No
gai_11_ASD_replication_cases-AU034904
Autism
17814274
17899608
85335
GRCh38
Deletion
No
morrow_08_ASD_discovery_cases-case1801
NA
ASD
NA
NA
17626000
17627000
300
Unknown
Deletion
No
pinto_14_ASD_discovery_cases2-case20128_4016001
N/A
M
ASD
Clinical profile: N/A.
Cognitive profile: N/A.
17596835
17627990
31156
GRCh38
Duplication
Yes
prasad_12_ASD_discovery_cases-case170300
NA
F
ASD
Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. CNV identified by previous SNP microarray study
16812763
16825093
12331
Unknown
Deletion
No
prasad_12_ASD_discovery_cases-case50005
NA
F
ASD
Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. CNV identified by previous SNP microarray study
17260455
17271386
10932
Unknown
Deletion
No
sanders_11_ASD_discovery_cases-11032.p1
5.8
M
Autism
NA
Full-scale IQ, 89; non-verbal IQ, 84; verbal IQ, 103
18036894
18038015
1122
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11196.p1
12.1
M
Autism
NA
Full-scale IQ, 112; non-verbal IQ, 117; verbal IQ, 106
17583312
17627990
44679
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-11220.p1
12.1
F
Autism
NA
Full-scale IQ, 80; non-verbal IQ, 87; verbal IQ, 75
17583312
17633234
49923
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-11346.p1
11
M
Autism
NA
Full-scale IQ, 133; non-verbal IQ, 132; verbal IQ, 121
17583312
17633234
49923
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-11455.p1
7.6
M
ASD
NA
Full-scale IQ, 68; non-verbal IQ, 73; verbal IQ, 69
17583312
17633234
49923
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-11580.p1
9.7
M
Autism
NA
Full-scale IQ, 78; non-verbal IQ, 88; verbal IQ, 64
17814274
17899608
85335
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11913.p1
4.5
F
Autism
NA
Full-scale IQ, 102; non-verbal IQ, 99; verbal IQ, 105
17269439
17280829
11391
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12240.p1
8.9
M
ASD
NA
Full-scale IQ, 91; non-verbal IQ, 86; verbal IQ, 104
17583312
17633234
49923
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-12272.p1
5.4
M
Autism
NA
Full-scale IQ, 70; non-verbal IQ, 79; verbal IQ, 62
17340379
17349866
9488
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12372.p1
15.7
F
Autism
NA
Full-scale IQ, 75; non-verbal IQ, 74; verbal IQ, 80
17583312
17632366
49055
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-12395.p1
5.2
M
Autism
NA
Full-scale IQ, 85; non-verbal IQ, 91; verbal IQ, 81
17296531
17303069
6539
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12582.p1
6.3
M
Autism
NA
Full-scale IQ, 57; non-verbal IQ, 73; verbal IQ, 45
17385350
17438393
53044
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12665.p1
9.3
M
Autism
NA
Full-scale IQ, 77; non-verbal IQ, 80; verbal IQ, 77
17591408
17632366
40959
GRCh38
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
engchuan_15_ASD_discovery_controls-control110036023109_
N/A
N/A
Control
No previous psychiatric history
17583312
17633234
49923
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-control110036024651_
N/A
N/A
Control
No previous psychiatric history
17583312
17633234
49923
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-control110036024685_
N/A
N/A
Control
No previous psychiatric history
17578504
17631210
52707
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-control110036025062_
N/A
N/A
Control
No previous psychiatric history
17578504
17633234
54731
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB123947_1007876030
N/A
N/A
Control
No previous psychiatric history
17583312
17634568
51257
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB299918_1007873981
N/A
N/A
Control
No previous psychiatric history
17583312
17633234
49923
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB462941_1007840754
N/A
N/A
Control
No previous psychiatric history
17583312
17633234
49923
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB488908_1007854765
N/A
N/A
Control
No previous psychiatric history
17583312
17633234
49923
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB501678_1007872289
N/A
N/A
Control
No previous psychiatric history
17156577
17208591
52015
GRCh38
Deletion
No
engchuan_15_ASD_discovery_controls-controlB610078_1007874586
N/A
N/A
Control
No previous psychiatric history
16937554
16982586
45033
GRCh38
Deletion
No
engchuan_15_ASD_discovery_controls-controlB665259_1007853930
N/A
N/A
Control
No previous psychiatric history
17583312
17634568
51257
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB928566_1007844750
N/A
N/A
Control
No previous psychiatric history
17583312
17633234
49923
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB979208_1007842459
N/A
N/A
Control
No previous psychiatric history
17583312
17633234
49923
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlHABC_900337_900337
N/A
N/A
Control
No previous psychiatric history
18312580
18359016
46437
GRCh38
Deletion
No
engchuan_15_ASD_discovery_controls-controlHABC_900362_900362
N/A
N/A
Control
No previous psychiatric history
17583312
17633061
49750
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlHABC_900736_900736
N/A
N/A
Control
No previous psychiatric history
17583312
17633061
49750
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlHABC_900918_900918
N/A
N/A
Control
No previous psychiatric history
17583312
17626618
43307
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlHABC_900972_900972
N/A
N/A
Control
No previous psychiatric history
16903448
16951646
48199
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlHABC_901144_901144
N/A
N/A
Control
No previous psychiatric history
17024443
17076369
51927
GRCh38
Deletion
No
engchuan_15_ASD_discovery_controls-controlHABC_902447_902447
N/A
N/A
Control
No previous psychiatric history
17586103
17633234
47132
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlHABC_902486_902486
N/A
N/A
Control
No previous psychiatric history
17586103
17633234
47132
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlHABC_902681_902681
N/A
N/A
Control
No previous psychiatric history
17583312
17632813
49502
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-11099.s1
14.5
F
Control (matched sibling)
NA
NA
17583312
17633234
49923
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-11196.s1
10
M
Control (matched sibling)
NA
NA
17583312
17631554
48243
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-11346.s1
12.9
M
Control (matched sibling)
NA
NA
17583312
17631554
48243
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-11455.s1
8.9
F
Control (matched sibling)
NA
NA
17583312
17633234
49923
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-11845.s1
7.5
F
Control (matched sibling)
NA
NA
16763142
16770636
7495
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-12197.s1
5.8
F
Control (matched sibling)
NA
NA
16638045
16651523
13479
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-12334.s1
4.2
M
Control (matched sibling)
NA
NA
17583312
17633234
49923
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-12372.s1
13.5
F
Control (matched sibling)
NA
NA
17583312
17632366
49055
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-12792.s1
5.8
F
Control (matched sibling)
NA
NA
17583312
17633234
49923
GRCh38
Duplication
No
sanders_11_ASD_discovery_controls-13159.s1
13.6
M
Control (matched sibling)
NA
NA
17904498
17911468
6971
GRCh38
Deletion
No
Cases
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
digregorio_17_DD/ID_discovery_cases-DECIPHER_300115
Unknown
RN7SL720P,RPS29P33,SAMM50P1,CNTLN
engchuan_15_ASD_discovery_cases-case13056_663
Unknown
engchuan_15_ASD_discovery_cases-case13211_2323
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_cases-case14342_4560
Unknown
ADAMTSL1
engchuan_15_ASD_discovery_cases-case16090_1571122001
Unknown
RN7SL720P,RPS29P33,CNTLN,BNC2
engchuan_15_ASD_discovery_cases-case20128_4016001
Unknown
SH3GL2
engchuan_15_ASD_discovery_cases-case20175_1679001
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_cases-case2211_1
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_cases-case4147_1
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_cases-case4381_1
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_cases-case6270_3
Unknown
ADAMTSL1
gai_11_ASD_discovery_cases-AU1099302
Inherited
0 genes
gai_11_ASD_discovery_cases-AU1099303
Inherited
0 genes
gai_11_ASD_replication_cases-AU034904
Inherited
morrow_08_ASD_discovery_cases-case1801
Maternal
NA
NA
SH3GL2
pinto_14_ASD_discovery_cases2-case20128_4016001
qPCR
Paternal
Simplex
(no siblings)
SH3GL2
prasad_12_ASD_discovery_cases-case170300
Unknown
Unknown
Unknown
BNC2
prasad_12_ASD_discovery_cases-case50005
Unknown
Unknown
Unknown
CNTLN
sanders_11_ASD_discovery_cases-11032.p1
Unknown
Simplex (quad-proband matched)
Segregated
ADAMTSL1
sanders_11_ASD_discovery_cases-11196.p1
Maternal
Simplex (quad-proband matched)
Not segregated
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_cases-11220.p1
Paternal
Simplex (quad-proband matched)
Not segregated
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_cases-11346.p1
Paternal
Simplex (quad-proband matched)
Not segregated
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_cases-11455.p1
Paternal
Simplex (quad-proband matched)
Not segregated
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_cases-11580.p1
Maternal
Simplex (quad-proband matched)
Segregated
sanders_11_ASD_discovery_cases-11913.p1
Paternal
Simplex (quad-proband matched)
Not segregated
CNTLN
sanders_11_ASD_discovery_cases-12240.p1
Paternal
Simplex (quad-proband matched)
Not segregated
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_cases-12272.p1
Paternal
Simplex (quad-proband matched)
Not segregated
CNTLN
sanders_11_ASD_discovery_cases-12372.p1
Maternal
Simplex (quad-proband matched)
Not segregated
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_cases-12395.p1
Maternal
Simplex (trio)
NA
CNTLN
sanders_11_ASD_discovery_cases-12582.p1
Unknown
Simplex (quad-proband matched)
Not segregated
CNTLN
sanders_11_ASD_discovery_cases-12665.p1
Paternal
Simplex (trio)
NA
SH3GL2
Controls
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
engchuan_15_ASD_discovery_controls-control110036023109_
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-control110036024651_
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-control110036024685_
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-control110036025062_
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlB123947_1007876030
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlB299918_1007873981
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlB462941_1007840754
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlB488908_1007854765
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlB501678_1007872289
Unknown
CNTLN
engchuan_15_ASD_discovery_controls-controlB610078_1007874586
Unknown
engchuan_15_ASD_discovery_controls-controlB665259_1007853930
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlB928566_1007844750
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlB979208_1007842459
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlHABC_900337_900337
Unknown
ADAMTSL1
engchuan_15_ASD_discovery_controls-controlHABC_900362_900362
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlHABC_900736_900736
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlHABC_900918_900918
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlHABC_900972_900972
Unknown
engchuan_15_ASD_discovery_controls-controlHABC_901144_901144
Unknown
RN7SL720P
engchuan_15_ASD_discovery_controls-controlHABC_902447_902447
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlHABC_902486_902486
Unknown
PABPC1P11,SH3GL2
engchuan_15_ASD_discovery_controls-controlHABC_902681_902681
Unknown
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_controls-11099.s1
Paternal
Simplex (quad)
NA
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_controls-11196.s1
Maternal
Simplex (quad)
NA
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_controls-11346.s1
Paternal
Simplex (quad)
NA
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_controls-11455.s1
Paternal
Simplex (quad)
NA
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_controls-11845.s1
Paternal
Simplex (quad)
NA
BNC2
sanders_11_ASD_discovery_controls-12197.s1
Paternal
Simplex (quad)
NA
BNC2
sanders_11_ASD_discovery_controls-12334.s1
Paternal
Simplex (quad)
NA
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_controls-12372.s1
Maternal
Simplex (quad)
NA
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_controls-12792.s1
Maternal
Simplex (quad)
NA
PABPC1P11,SH3GL2
sanders_11_ASD_discovery_controls-13159.s1
Both parents
Simplex (quad)
NA
ADAMTSL1
No Animal Model Data Available