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8q24.12CNV Type: Deletion-Duplication


Largest CNV size: 47532 bp

Statistics Box:
Number of Reports: 5



Summary Information

Summary statement in development

Additional Locus Information

Genome browsers

USCS Symbol             NCBI Symbol

Decipher

            Decipher Symbol

References

Major Reports

Title
Author, Year
Report Class
CNV Type

No Major Reports

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
A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Duplication
Transmission disequilibrium of small CNVs in simplex autism.
Deletion
Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation.
Duplication
Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.
Duplication

Cases

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 brand_15_ASD_discovery_cases
 ASD cases who had been previously been screened by CNVs by CMA as part of the Simons Simplex Collection (SSC) in Sanders et al., 2011
 259
 Diagnosis of ASD
 N/A
 N/A
 31815
 0
 2
 2
 krumm_13_ASD_discovery_cases
 Probands from quad families ascertained as part of the Simons Simplex Collection (SSC); CNVs detected using data from four previously published exome sequencing studies (O'Roak et al., 2011; Iossifov et al., 2012; O'Roak et al., 2012; Sanders et al., 2012)
 411
 Diagnosis of ASD. Social Responsiveness Scale (SRS) used as a quantitative measure of social deficits
 N/A
 81.265% Male
 106229
 1
 0
 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
 92739
 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
 47532
 13
 4
 17
 yin_16_ASD_discovery_cases
 Discovery cohort of ASD cases recruited from the Department of Psychiatry of National Taiwan University Hospital (NTUH), Chang Gung Memorial Hospital (CGMH), Taoyuan, and Taoyuan Mental Hospital (TMH), Taiwan.
 335
 Cases diagnosed with autistic disorder according to DSM-IV and confirmed by using the Chinese version of ADI-R. Cases' autistic behaviors assessed by Social Responsiveness Scale (SRS), and cognitive functions assessed by the Weschler Intelligence Scale for Children-Third Edition (WISC-III) and the Wisconsin Card Sorting Test (WCST).
 Mean, 9.39 4.04 yrs.
 89.3% Male
 71595
 0
 2
 2

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
 102663
 0
 2
 2
 krumm_13_ASD_discovery_controls
 Unaffected siblings of ASD probands from quad families ascertained as part of the Simons Simplex Collection (SSC); CNVs detected using data from four previously published exome sequencing studies (O'Roak et al., 2011; Iossifov et al., 2012; O'Roak et al., 2012; Sanders et al., 2012)
 411
 Control (unaffected siblings of ASD probands). Social Responsiveness Scale (SRS) used as a quantitative measure of social deficits
 N/A
 46.47% Male
 220516
 1
 0
 1
 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.
 
 27178
 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)
 92739
 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.
 
 26877
 6
 3
 9
 yin_16_ASD_discovery_controls
 Individuals from the Han Chinese Cell and Genome Bank (HCCGB) in Taiwan
 1093
 Controls
 Mean, 68.07 10.12 yrs.
 48.0% Male
 71595
 0
 0
 0

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 brand_15_ASD_discovery_cases
  N/A
 Long-insert WGS
  Long-insert whole genome sequencing
 LUMPY, cn.MOPS, SV classifier
 
 None
 krumm_13_ASD_discovery_cases
  N/A
 WES
  Whole exome sequencing platforms used in four recent publications (O'Roak et al., 2011; Sanders et al., 2012; O'Roak et al., 2012, and Iossifov et al., 2012)
 DNACopy, CGHCall
 CoNIFER
 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
 
 
 yin_16_ASD_discovery_cases
  Han Chinese
 Array SNP
  Affymetrix 6.0
 
 Affymetrix Genotyping Console v.4.1
 None

Controls

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
  engchuan_15_ASD_discovery_controls
  Caucasian
  Solid phase hybridization
  Illumina 1M
 
 
  None
  krumm_13_ASD_discovery_controls
  N/A
  WES
  Whole exome sequencing platforms used in four recent publications (O'Roak et al., 2011; Sanders et al., 2012; O'Roak et al., 2012, and Iossifov et al., 2012)
  DNACopy, CGHCall
  CoNIFER
  None
  nord_11_ASD_discovery_controls
 
  aCGH
  NimbleGen HD2
  Sliding-window algorithm, ~10 kb minumum size threshold
 
  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
 
 
  yin_16_ASD_discovery_controls
  Han Chinese
  Array SNP
  Affymetrix 6.0
 
  Affymetrix Genotyping Console v.4.1
  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
  brand_15_ASD_discovery_cases-case15
 N/A
 N/A
 ASD
 Long-insert WGS identified a dupINVdup involving chromosome 8 in this case. Duplication previously identified by aCGH (chr8:122320560-122341946; hg19).
 
 121307206
 121333404
  26199
 GRCh38
 Duplication
 No
  brand_15_ASD_discovery_cases-case15
 N/A
 N/A
 ASD
 Long-insert WGS identified a dupINVdup involving chromosome 8 in this case. Duplication previously identified by aCGH (chr8:122405097-122426082; hg19).
 
 121387710
 121419525
  31816
 GRCh38
 Duplication
 No
  krumm_13_ASD_discovery_cases-case14110.p1
 N/A
 M
 ASD
 ASD proband from SSC quad family 14110. SRS score of 69.
 Full-scale IQ (FSIQ) score of 77.
 119744287
 119850516
  106230
 GRCh38
 Deletion
 No (not tested)
  prasad_12_ASD_discovery_cases-case93736
 NA
 M
 ASD
 Diagnosis of ASD based on meeting criteria on ADI-R and/or ADOS. CNV identified by previous SNP microarray study
 
 121552138
 121644876
  92739
 Unknown
 Duplication
 No
  sanders_11_ASD_discovery_cases-11165.p1
 5.2
 M
 Autism
 NA
 Full-scale IQ, 104; non-verbal IQ, 112; verbal IQ 89
 118725045
 118772577
  47533
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11409.p1
 4.1
 M
 Autism
 NA
 Full-scale IQ, 96; non-verbal IQ, 101; verbal IQ 90
 119007354
 119013102
  5749
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11447.p1
 6.6
 M
 Autism
 NA
 Full-scale IQ, 89; non-verbal IQ, 97; verbal IQ, 82
 119007354
 119015632
  8279
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11475.p1
 7.8
 M
 Autism
 NA
 Full-scale IQ, 94; non-verbal IQ, 86; verbal IQ, 110
 119007354
 119013102
  5749
 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
 119007354
 119013102
  5749
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11794.p1
 8.3
 M
 Autism
 NA
 Full-scale IQ, 36; non-verbal IQ, 40; verbal IQ, 33
 119007354
 119017470
  10117
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-11794.p1
 8.3
 M
 Autism
 NA
 Full-scale IQ, 36; non-verbal IQ, 40; verbal IQ, 33
 121392857
 121413842
  20986
 GRCh38
 Duplication
 No
  sanders_11_ASD_discovery_cases-11794.p1
 8.3
 M
 Autism
 NA
 Full-scale IQ, 36; non-verbal IQ, 40; verbal IQ, 33
 121308320
 121329706
  21387
 GRCh38
 Duplication
 No
  sanders_11_ASD_discovery_cases-11794.p1
 8.3
 M
 Autism
 NA
 Full-scale IQ, 36; non-verbal IQ, 40; verbal IQ, 33
 119245946
 119274653
  28708
 GRCh38
 Duplication
 No
  sanders_11_ASD_discovery_cases-12102.p1
 5.1
 M
 Autism
 NA
 Full-scale IQ, 45; non-verbal IQ, 52; verbal IQ, 38
 119007354
 119015632
  8279
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12221.p1
 4.1
 M
 Autism
 NA
 Full-scale IQ, 89; non-verbal IQ, 99; verbal IQ, 76
 119253601
 119267398
  13798
 GRCh38
 Duplication
 No
  sanders_11_ASD_discovery_cases-12260.p1
 5.3
 M
 Autism
 NA
 Full-scale IQ, 106; non-verbal IQ, 103; verbal IQ, 109
 119007354
 119013102
  5749
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12424.p1
 4.2
 M
 ASD
 NA
 Full-scale IQ, 69; non-verbal IQ, 77; verbal IQ, 65
 119007354
 119013102
  5749
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12717.p1
 11.1
 M
 Autism
 NA
 Full-scale IQ, 89; non-verbal IQ, 94; verbal IQ, 86
 119007354
 119017470
  10117
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12757.p1
 5.3
 M
 Autism
 NA
 Full-scale IQ, 57; non-verbal IQ, 62; verbal IQ, 55
 119007354
 119013102
  5749
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-12964.p1
 6.9
 M
 Autism
 NA
 Full-scale IQ, 38; non-verbal IQ, 48; verbal IQ, 28
 119007354
 119015632
  8279
 GRCh38
 Deletion
 No
  sanders_11_ASD_discovery_cases-13013.p1
 8.1
 M
 Autism
 NA
 Full-scale IQ, 72; non-verbal IQ, 68; verbal IQ, 86
 119007354
 119013102
  5749
 GRCh38
 Deletion
 No
  yin_16_ASD_discovery_cases-case327
 N/A
 N/A
 ASD
 Cases diagnosed with autistic disorder according to DSM-IV and confirmed by using the Chinese version of ADI-R.
 
 118576018
 118577134
  1117
 GRCh38
 Duplication
 No
  yin_16_ASD_discovery_cases-case328
 N/A
 N/A
 ASD
 Cases diagnosed with autistic disorder according to DSM-IV and confirmed by using the Chinese version of ADI-R.
 
 120364045
 120435638
  71594
 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-control110036018745_
  N/A
  N/A
  Control
  No previous psychiatric history
 
  121314683
  121417346
  102664
  GRCh38
  Duplication
  No
  engchuan_15_ASD_discovery_controls-control110036022051_
  N/A
  N/A
  Control
  No previous psychiatric history
 
  121316932
  121386627
  69696
  GRCh38
  Duplication
  No
  krumm_13_ASD_discovery_controls-control14110.s1
  N/A
  F
  Control
  Unaffected sibling from SSC quad family 14110. SRS score of 39.
 
  119626564
  119847080
  220517
  GRCh38
  Deletion
  No (not tested)
  nord_11_ASD_discovery_controls-04C27265
 
 
  Control
 
 
  121935857
  121963034
  27178
  Unknown
  Deletion
 
  sanders_11_ASD_discovery_controls-11564.s1
  6.3
  F
  Control (matched sibling)
  NA
  NA
  119007354
  119015632
  8279
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-11794.s1
  4.3
  F
  Control (matched sibling)
  NA
  NA
  119007354
  119013102
  5749
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-11941.s1
  8.7
  F
  Control (matched sibling)
  NA
  NA
  119007354
  119013102
  5749
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-12220.s1
  16.1
  M
  Control (matched sibling)
  NA
  NA
  121308320
  121335197
  26878
  GRCh38
  Duplication
  No
  sanders_11_ASD_discovery_controls-12261.s1
  21.5
  M
  Control (matched sibling)
  NA
  NA
  119007354
  119013102
  5749
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-12424.s1
  6.2
  F
  Control (matched sibling)
  NA
  NA
  119007354
  119013102
  5749
  GRCh38
  Deletion
  No
  sanders_11_ASD_discovery_controls-12617.s1
  14.6
  M
  Control (matched sibling)
  NA
  NA
  121308320
  121329706
  21387
  GRCh38
  Duplication
  No
  sanders_11_ASD_discovery_controls-12617.s1
  14.6
  M
  Control (matched sibling)
  NA
  NA
  121392857
  121417346
  24490
  GRCh38
  Duplication
  No
  sanders_11_ASD_discovery_controls-13166.s1
  5.6
  M
  Control (matched sibling)
  NA
  NA
  119007354
  119013102
  5749
  GRCh38
  Deletion
  No

Cases

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
 brand_15_ASD_discovery_cases-case15
 
 
 Paternal
 Simplex
 Unknown
 
 
 brand_15_ASD_discovery_cases-case15
 
 
 Paternal
 Simplex
 Unknown
 
 
 krumm_13_ASD_discovery_cases-case14110.p1
 
 
 Paternal
 Simplex
 Not segregated
 DSCC1,TAF2
 
 prasad_12_ASD_discovery_cases-case93736
 
 
 Unknown
 Unknown
 Unknown
 MTBP,SNTB1
 
 sanders_11_ASD_discovery_cases-11165.p1
 
 
 Paternal
 Simplex (trio)
 NA
 RPS26P35,SAMD12-AS1
 
 sanders_11_ASD_discovery_cases-11409.p1
 
 
 Maternal
 Simplex (trio)
 NA
 COLEC10
 
 sanders_11_ASD_discovery_cases-11447.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Segregated
 COLEC10
 
 sanders_11_ASD_discovery_cases-11475.p1
 
 
 Both parents
 Simplex (quad-proband matched)
 Segregated
 COLEC10
 
 sanders_11_ASD_discovery_cases-11564.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Not segregated
 COLEC10
 
 sanders_11_ASD_discovery_cases-11794.p1
 
 
 Both parents
 Simplex (quad-proband matched)
 Segregated
 COLEC10
 
 sanders_11_ASD_discovery_cases-11794.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 
 
 sanders_11_ASD_discovery_cases-11794.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 
 
 sanders_11_ASD_discovery_cases-11794.p1
 
 
 Maternal
 Simplex (quad-proband matched)
 Segregated
 MAL2-AS1
 
 sanders_11_ASD_discovery_cases-12102.p1
 
 
 Paternal
 Simplex (trio)
 NA
 COLEC10
 
 sanders_11_ASD_discovery_cases-12221.p1
 
 
 Paternal
 Simplex (quad-proband unmatched)
 Unknown
 
 
 sanders_11_ASD_discovery_cases-12260.p1
 
 
 Maternal
 Simplex (trio)
 NA
 COLEC10
 
 sanders_11_ASD_discovery_cases-12424.p1
 
 
 Both parents
 Simplex (quad-proband matched)
 Not segregated
 COLEC10
 
 sanders_11_ASD_discovery_cases-12717.p1
 
 
 Maternal
 Simplex (trio)
 NA
 COLEC10
 
 sanders_11_ASD_discovery_cases-12757.p1
 
 
 Paternal
 Simplex (trio)
 NA
 COLEC10
 
 sanders_11_ASD_discovery_cases-12964.p1
 
 
 Paternal
 Simplex (quad-proband matched)
 Not segregated
 COLEC10
 
 sanders_11_ASD_discovery_cases-13013.p1
 
 
 Both parents
 Simplex (trio)
 NA
 COLEC10
 
 yin_16_ASD_discovery_cases-case327
 
 
 Unknown
 Unknown
 Unknown
 SAMD12
 
 yin_16_ASD_discovery_cases-case328
 
 
 Unknown
 Unknown
 Unknown
 MRPL13,COL14A1
 

Controls

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
engchuan_15_ASD_discovery_controls-control110036018745_
 
 
  Unknown
 
 
  RPL35AP19
 
engchuan_15_ASD_discovery_controls-control110036022051_
 
 
  Unknown
 
 
  RPL35AP19
 
krumm_13_ASD_discovery_controls-control14110.s1
 
 
  Paternal
  Simplex
 
  RN7SKP153,DSCC1,ENPP2,TAF2
 
nord_11_ASD_discovery_controls-04C27265
 
 
 
 
 
  0 genes
 
sanders_11_ASD_discovery_controls-11564.s1
 
 
  Maternal
  Simplex (quad)
  NA
  COLEC10
 
sanders_11_ASD_discovery_controls-11794.s1
 
 
  Both parents
  Simplex (quad)
  NA
  COLEC10
 
sanders_11_ASD_discovery_controls-11941.s1
 
 
  Paternal
  Simplex (quad)
  NA
  COLEC10
 
sanders_11_ASD_discovery_controls-12220.s1
 
 
  Paternal
  Simplex (quad)
  NA
 
 
sanders_11_ASD_discovery_controls-12261.s1
 
 
  Paternal
  Simplex (quad)
  NA
  COLEC10
 
sanders_11_ASD_discovery_controls-12424.s1
 
 
  Both parents
  Simplex (quad)
  NA
  COLEC10
 
sanders_11_ASD_discovery_controls-12617.s1
 
 
  Paternal
  Simplex (quad)
  NA
 
 
sanders_11_ASD_discovery_controls-12617.s1
 
 
  Paternal
  Simplex (quad)
  NA
 
 
sanders_11_ASD_discovery_controls-13166.s1
 
 
  Paternal
  Simplex (quad)
  NA
  COLEC10
 

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