5q34CNV Type: Deletion-Duplication
Largest CNV size: 519629 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
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabili...
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
Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Deletion
A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Deletion
Copy number variation in Han Chinese individuals with autism spectrum disorder.
Duplication
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
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
669785
5
2
7
gazzellone_14_ASD_discovery_cases
ASD-affected individuals referred to the Children Development and Behavior Research Center (CDRBC) at Harbin Medical University, China, between January 2007 and June 2011.
104
Diagnosis of ASD made using Autism Behavior Checklist (ABC) and Childhood Autism Rating Scale (CARS)
Mean age at enrollment, 4.31 1.80 yrs.
87.5% Male
89707
0
1
1
girirajan_11_ASD_discovery_cases
ASD cases with sporadic autism from the Simons Simplex Collection (SSC)
336
Diagnosis of ASD based on meeting criteria on ADOS, ADI-R, and expert clinical judgment. 246 cases with no intellectual disability, 90 cases with intellectual disability. Exclusion criteria: significant hearing, vision, or motor problems; significant birth complications; a diagnosis of ASD-related disorders, such as Fragile X; or having a relative (up to 3rd degree) with ASD or sibling showing ASD-related symptoms.
471267
1
0
1
kaminsky_11_DD/ID/ASD_discovery_cases
Cases from the International Standards for Cytogenomic Arrays (ISCA) consortium
15749
Unexplained developmental delay, intellectual disability, dysmorphic features, multiple congenital anomalies, autism spectrum disorders, or clinical features suggestive of a chromosomal syndrome
NA
NA
2176962
2
0
2
maini_18_ASD/DD/ID_discovery_cases
Patients evaluated at the Clinical Genetics Unit of Arcispedale Santa Maria Nuova, AUSL-IRCCS of Reggio Emilia that were investigated through aCGH between 2005 and 2016
293
Cases presented with one or more neurodevelopmental disorders (NDD), multiple congenital anomalies (MCA), and/or dysmorphic features. Most frequent neurodevelopmental diagnoses include language delay (78.5%), intellectual disability (66.4%), motor delay (50.7%), and ASD (13.9%); dysmorphic features were also frequently observed (52.7%)
Mean age, 7 yrs. (range, 1 mo.-29 yrs.)
57.5% Male
302000
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
35349
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
519629
12
5
17
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
100439
3
3
6
girirajan_11_ASD_discovery_controls
Control individuals ascertained by NIMH Genetics Initiative. DNA samples from these individuals were obtained from the Rutgers Univ. Cell & DNA Repository.
337
Control. Individuals screened specifically for eight mental health disorders.
1445514
0
1
1
kaminsky_11_DD/ID/ASD_discovery_controls
Controls from the International Standards for Cytogenomic Arrays (ISCA) consortium
10118
Controls
NA
NA
NA
NA
NA
NA
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.
21040
2
0
2
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)
10934
1
0
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)
35349
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.
513533
9
0
9
Cases
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
engchuan_15_ASD_discovery_cases
Caucasian
Solid phase hybridization
Illumina 1M
None
gazzellone_14_ASD_discovery_cases
Han Chinese
Array SNP
Affymetrix CytoScan HD
ChAS, iPattern, Nexus, Partek
None
girirajan_11_ASD_discovery_cases
aCGH
Custom microarray targeting 107 genomic hotspot regions (Roche NimbleGen Hotspot v1.0 array; 12 x 135K)
HMM
None
kaminsky_11_DD/ID/ASD_discovery_cases
NA
aCGH
Agilent 44K, Agilent 105K
Feature Extraction, DNA Analytics
FISH, qPCR, MLPA, aCGH, standard G-banded chromosome analysis
maini_18_ASD/DD/ID_discovery_cases
Italian
aCGH, array SNP
Multiple platforms, including Agilent and Affymetrix arrays (8x60K oligochips since 2012)
None
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
girirajan_11_ASD_discovery_controls
aCGH
Custom microarray targeting 107 genomic hotspot regions (Roche NimbleGen Hotspot v1.0 array; 12 x 135K)
HMM
None
kaminsky_11_DD/ID/ASD_discovery_controls
NA
aCGH
Agilent 44K, Agilent 105K
Feature Extraction, DNA Analytics
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
qPCR
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
engchuan_15_ASD_discovery_cases-case14394_5030
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
163205609
163295548
89940
GRCh38
Deletion
No
engchuan_15_ASD_discovery_cases-case17033_1
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
166017040
166139387
122348
GRCh38
Deletion
No
engchuan_15_ASD_discovery_cases-case3194_4
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
161118834
161161554
42721
GRCh38
Duplication
No
engchuan_15_ASD_discovery_cases-case3266_3
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
162824414
162962564
138151
GRCh38
Deletion
No
engchuan_15_ASD_discovery_cases-case3586_3
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
166351889
167021674
669786
GRCh38
Duplication
No
engchuan_15_ASD_discovery_cases-case4201_1
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
163321598
163399607
78010
GRCh38
Deletion
No
engchuan_15_ASD_discovery_cases-case4221_1
N/A
N/A
ASD
Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
163321598
163374070
52473
GRCh38
Deletion
No
gazzellone_14_ASD_discovery_cases-case693-3
N/A
M
ASD
ASD; no other clinical information provided
N/A
164614743
164704450
89708
GRCh38
Duplication
No
girirajan_11_ASD_discovery_cases-Si89
17
M
Autism
ADOS score: 10. Vineland composite score: 60.
Moderate mental retardation/intellectual disability. Full-scale IQ, 43; Verbal IQ, 32; Non-verbal IQ, 62.
166376090
166847357
471268
GRCh38
Deletion
No
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004318
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
161709251
162161606
452356
GRCh38
Deletion
Yes
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004642
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
161909955
164086917
2176963
GRCh38
Deletion
Yes
maini_18_ASD/DD/ID_discovery_cases-case_unknown180
N/A
N/A
NDD/MCA/dysmorphic features
CNV was identified in an individual with one or more neurodevelopmental disorders (NDD), multiple congenital anomalies (MCA), and/or dysmorphic features (detailed clinical information was not available). CNV classified as variant of unknown significance-likely benign (VOUS-LB)
167268295
167570526
302232
GRCh38
Duplication
No
prasad_12_ASD_discovery_cases-case78391
NA
F
ASD
Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. CNV identified by previous SNP microarray study
165637262
165672610
35349
Unknown
Deletion
No
prasad_12_ASD_discovery_cases-case87750
NA
M
ASD
Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. Novel CNV
167023982
167030333
6352
Unknown
Deletion
No
sanders_11_ASD_discovery_cases-11110.p1
15.8
M
Autism
NA
Full-scale IQ, 43; non-verbal IQ, 62; verbal IQ, 32
166348726
166868355
519630
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11258.p1
14.8
M
Autism
NA
Full-scale IQ, 108; non-verbal IQ, 119; verbal IQ, 96
163311832
163386301
74470
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11339.p1
10
F
Autism
NA
Full-scale IQ, 72; non-verbal IQ, 62; verbal IQ, 93
161114420
161121367
6948
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11424.p1
6.8
M
Autism
NA
Full-scale IQ, 92; non-verbal IQ, 97; verbal IQ, 90
166417719
166442998
25280
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-11501.p1
11.3
M
Autism
NA
Full-scale IQ, 78; non-verbal IQ, 79; verbal IQ, 71
163127792
163147002
19211
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11564.p1
10.8
M
Autism
NA
Full-scale IQ, 94; non-verbal IQ, 89; verbal IQ, 106
166412688
166417719
5032
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11720.p1
8
M
ASD
NA
Full-scale IQ, 68; non-verbal IQ, 82; verbal IQ, 51
163974400
163982203
7804
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-11825.p1
6.6
M
Autism
NA
Full-scale IQ, 131; non-verbal IQ, 135; verbal IQ, 115
166293601
166306612
13012
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-11888.p1
4
M
ASD
NA
Full-scale IQ, 81; non-verbal IQ, 89; verbal IQ, 75
160823993
160848486
24494
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12448.p1
10.5
M
Autism
NA
Full-scale IQ, 108; non-verbal IQ, 104; verbal IQ, 116
163974400
163991850
17451
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-12667.p1
6.3
M
Autism
NA
Full-scale IQ, 34; non-verbal IQ, 49; verbal IQ, 19
163974400
163991850
17451
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-12786.p1
7
M
Autism
NA
Full-scale IQ, 88; non-verbal IQ, 90; verbal IQ, 87
165016088
165087875
71788
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12864.p1
5.8
F
Autism
NA
Full-scale IQ, 67; non-verbal IQ, 65; verbal IQ, 81
167655000
167659790
4791
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-12921.p1
11.4
M
Autism
NA
Full-scale IQ, 80; non-verbal IQ, 74; verbal IQ, 100
164973535
165016088
42554
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-13001.p1
6.3
M
Autism
NA
Full-scale IQ, 72; non-verbal IQ, 91; verbal IQ, 46
163748147
163754959
6813
GRCh38
Deletion
No
sanders_11_ASD_discovery_cases-13166.p1
9.1
M
Autism
NA
Full-scale IQ, 46; non-verbal IQ, 47; verbal IQ, 45
166097385
166139387
42003
GRCh38
Duplication
No
sanders_11_ASD_discovery_cases-13382.p1
4.3
M
Autism
NA
Full-scale IQ, 76; non-verbal IQ, 74; verbal IQ, 83
160636520
160652221
15702
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
engchuan_15_ASD_discovery_controls-controlB239915_1007841983
N/A
N/A
Control
No previous psychiatric history
164895047
164944745
49699
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB658740_1007854250
N/A
N/A
Control
No previous psychiatric history
161115167
161164269
49103
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlB742453_1007844402
N/A
N/A
Control
No previous psychiatric history
163321598
163374070
52473
GRCh38
Deletion
No
engchuan_15_ASD_discovery_controls-controlB991945_1007873310
N/A
N/A
Control
No previous psychiatric history
163321598
163374070
52473
GRCh38
Deletion
No
engchuan_15_ASD_discovery_controls-controlHABC_901043_901043
N/A
N/A
Control
No previous psychiatric history
161115167
161161554
46388
GRCh38
Duplication
No
engchuan_15_ASD_discovery_controls-controlHABC_902884_902884
N/A
N/A
Control
No previous psychiatric history
162203280
162303719
100440
GRCh38
Deletion
No
girirajan_11_ASD_discovery_controls-NIMH_245
NA
NA
Control
NA
NA
163816371
165261885
1445515
GRCh38
Duplication
No
nord_11_ASD_discovery_controls-04C27344
Control
165697501
165711420
13920
Unknown
Deletion
nord_11_ASD_discovery_controls-04C27965
Control
165648681
165669720
21040
Unknown
Deletion
poultney_13_ASD_discovery_controls-control04C28575A
N/A
F
Control
NIMH Control (NIMH ID 75492)
168506019
168516952
10934
GRCh38
Deletion
Yes
sanders_11_ASD_discovery_controls-11093.s1
9.8
M
Control (matched sibling)
NA
NA
166340689
166351889
11201
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-11110.s1
16.8
M
Control (matched sibling)
NA
NA
166348726
166862259
513534
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-11258.s1
10.8
F
Control (matched sibling)
NA
NA
163321598
163402942
81345
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-11765.s1
7.8
F
Control (matched sibling)
NA
NA
166340689
166351889
11201
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-12597.s1
5.3
F
Control (matched sibling)
NA
NA
162293367
162303081
9715
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-12708.s1
11.8
F
Control (matched sibling)
NA
NA
166341961
166351889
9929
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-12864.s1
12.9
F
Control (matched sibling)
NA
NA
167655000
167659790
4791
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-12894.s1
4.9
F
Control (matched sibling)
NA
NA
160823993
160848486
24494
GRCh38
Deletion
No
sanders_11_ASD_discovery_controls-12921.s1
6.5
F
Control (matched sibling)
NA
NA
164973535
165016088
42554
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-case14394_5030
Unknown
engchuan_15_ASD_discovery_cases-case17033_1
Unknown
RPL7P20
engchuan_15_ASD_discovery_cases-case3194_4
Unknown
engchuan_15_ASD_discovery_cases-case3266_3
Unknown
engchuan_15_ASD_discovery_cases-case3586_3
Unknown
LINC01947
engchuan_15_ASD_discovery_cases-case4201_1
Unknown
engchuan_15_ASD_discovery_cases-case4221_1
Unknown
gazzellone_14_ASD_discovery_cases-case693-3
Unknown
Unknown
Unknown
girirajan_11_ASD_discovery_cases-Si89
Unknown
Simplex
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004318
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Maternal
Unknown
Unknown
GLRXP3,LINC01202,GABRA1,GABRG2
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004642
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
RNU6-164P,ARL2BPP5,MRPL57P6,CCNG1,HMMR-AS1,RNU6-168P,LSM1P2,LINC01202,HMMR,MAT2B,GABRG2,NUDCD2
maini_18_ASD/DD/ID_discovery_cases-case_unknown180
Unknown
Unknown
Unknown
TENM2
prasad_12_ASD_discovery_cases-case78391
Unknown
Unknown
Unknown
0 genes
prasad_12_ASD_discovery_cases-case87750
Unknown
Unknown
Unknown
ODZ2
sanders_11_ASD_discovery_cases-11110.p1
Maternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-11258.p1
Maternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-11339.p1
Paternal
Simplex (quad-proband matched)
Segregated
sanders_11_ASD_discovery_cases-11424.p1
Maternal
Simplex (quad-proband matched)
Segregated
sanders_11_ASD_discovery_cases-11501.p1
Maternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-11564.p1
Paternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-11720.p1
Maternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-11825.p1
Paternal
Simplex (trio)
NA
sanders_11_ASD_discovery_cases-11888.p1
Maternal
Simplex (quad-proband matched)
Not segregated
ATP10B
sanders_11_ASD_discovery_cases-12448.p1
Maternal
Simplex (trio)
NA
sanders_11_ASD_discovery_cases-12667.p1
Maternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-12786.p1
Unknown
Simplex (quad-proband matched)
Segregated
sanders_11_ASD_discovery_cases-12864.p1
Maternal
Simplex (quad-proband matched)
Not segregated
TENM2
sanders_11_ASD_discovery_cases-12921.p1
Maternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-13001.p1
Maternal
Simplex (quad-proband matched)
Not segregated
sanders_11_ASD_discovery_cases-13166.p1
Paternal
Simplex (quad-proband matched)
Segregated
sanders_11_ASD_discovery_cases-13382.p1
Paternal
Simplex (trio)
NA
ATP10B
Controls
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
engchuan_15_ASD_discovery_controls-controlB239915_1007841983
Unknown
RNU6-209P
engchuan_15_ASD_discovery_controls-controlB658740_1007854250
Unknown
engchuan_15_ASD_discovery_controls-controlB742453_1007844402
Unknown
engchuan_15_ASD_discovery_controls-controlB991945_1007873310
Unknown
engchuan_15_ASD_discovery_controls-controlHABC_901043_901043
Unknown
engchuan_15_ASD_discovery_controls-controlHABC_902884_902884
Unknown
girirajan_11_ASD_discovery_controls-NIMH_245
Unknown
LSM1P2,RNU6-209P,LINC02143,LINC01938
nord_11_ASD_discovery_controls-04C27344
0 genes
nord_11_ASD_discovery_controls-04C27965
0 genes
poultney_13_ASD_discovery_controls-control04C28575A
qPCR
Unknown
RARS
sanders_11_ASD_discovery_controls-11093.s1
Maternal
Simplex (quad)
NA
sanders_11_ASD_discovery_controls-11110.s1
Maternal
Simplex (quad)
NA
sanders_11_ASD_discovery_controls-11258.s1
Maternal
Simplex (quad)
NA
sanders_11_ASD_discovery_controls-11765.s1
Paternal
Simplex (quad)
NA
sanders_11_ASD_discovery_controls-12597.s1
Paternal
Simplex (quad)
NA
sanders_11_ASD_discovery_controls-12708.s1
Maternal
Simplex (quad)
NA
sanders_11_ASD_discovery_controls-12864.s1
Maternal
Simplex (quad)
NA
TENM2
sanders_11_ASD_discovery_controls-12894.s1
Paternal
Simplex (quad)
NA
ATP10B
sanders_11_ASD_discovery_controls-12921.s1
Maternal
Simplex (quad)
NA
No Animal Model Data Available