AutismKB 2.0

View CNVs/SVs


View by Evidence Type: de novo CNVs ( CNVs Only Present In Patients   de novo CNVs   Overlapping/Recurrent CNVs  
                                        CNVs Overlapping With ACRD   CNVs Not Present In Control   Significant Enriched CNVs   Others  All  )


View by Chromosome:15 ( 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X  Y  All  )


Notes: ACRD: Autism Chromosome Rearrangement Database
CNV Name Chr Band Gain/Loss Number of CNVs Evidence Type Reference
Case Control
AutCNV0004563 15 15q11.1 Loss 1 - de novo CNVs; Patircia, 2011
AutCNV0004564 15 15q11.1-q11.2 Loss 1 - de novo CNVs; Patircia, 2011
AutCNV0004565 15 15q11.2 Loss 1 - de novo CNVs; Patircia, 2011
AutCNV0004566 15 15q13.2 Loss 1 - de novo CNVs; Patircia, 2011
AutCNV0004567 15 15q13.3 Loss 1 - de novo CNVs; Patircia, 2011
AutCNV0004785 15 15q11q12 gain - - CNVs Only Present In Patients; de novo CNVs; Nava C, 2014
AutCNV0004851 15 15q13.2-q13.3 loss - - CNVs Only Present In Patients; de novo CNVs; Moreira DP, 2014
AutCNV0004908 15 15q11.2 gain - - CNVs Only Present In Patients; de novo CNVs; Castronovo C, 2015
AutCNV0004909 15 15q11.213.1 gain - - CNVs Only Present In Patients; de novo CNVs; Castronovo C, 2015
AutCNV0004979 15 15q11.2-13.1 - - - CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; Sanders SJ, 2015
AutCNV0004980 15 15q12 - - - CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; Sanders SJ, 2015
AutCNV0004981 15 15q13.2-13.3 - - - CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; Sanders SJ, 2015
AutCNV0005635 15 15 - - - de novo CNVs; Krumm N, 2015
AutCNV0005643 15 15 - - - de novo CNVs; Krumm N, 2015
AutCNV0005649 15 15 - - - de novo CNVs; Krumm N, 2015
AutCNV0005650 15 15 - - - de novo CNVs; Krumm N, 2015
AutCNV0005651 15 15 - - - de novo CNVs; Krumm N, 2015
AutCNV0005655 15 15 - - - de novo CNVs; Krumm N, 2015
AutCNV0005656 15 15 - - - de novo CNVs; Krumm N, 2015
AutCNV0005920 15 15q11.2 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005921 15 15q11.2-q13.1 gain - - de novo CNVs; Brandler WM, 2018
AutCNV0005922 15 15q13.1-q13.3 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005923 15 15q26.1 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005944 15 15q11.2-q13.1 gain - - de novo CNVs; Brandler WM, 2018
AutCNV0005946 15 15q13.1-q13.3 loss - - de novo CNVs; Brandler WM, 2018

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Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018