AutismKB 2.0

View CNVs/SVs


View by Evidence Type: All ( 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
AutCNV0004851 15 15q13.2-q13.3 loss - - CNVs Only Present In Patients; de novo CNVs; Moreira DP, 2014
AutCNV0004852 15 15q13.3 gain - - CNVs Only Present In Patients; Moreira DP, 2014
AutCNV0004853 15 15q13.3 gain - - CNVs Only Present In Patients; Moreira DP, 2014
AutCNV0004863 15 15q11.2 loss - - CNVs Only Present In Patients; 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
AutCNV0004911 15 15q13.3 loss - - CNVs Only Present In Patients; Overlapping/Recurrent CNVs; Lowther C, 2015
AutCNV0004914 15 - gain - - CNVs Only Present In Patients; Tammimies K, 2015
AutCNV0004949 15 - gain - - CNVs Only Present In Patients; Brand H, 2015
AutCNV0004960 15 - gain - - CNVs Only Present In Patients; Brand H, 2015
AutCNV0004964 15 15q12 gain 28 0 CNVs Only Present In Patients; Significant Enriched CNVs; Hadley D, 2014
AutCNV0004965 15 15q12 gain 27 1 CNVs Only Present In Patients; Significant Enriched CNVs; Hadley D, 2014
AutCNV0004966 15 15q13.1 gain 24 0 CNVs Only Present In Patients; Significant Enriched CNVs; Hadley D, 2014
AutCNV0004968 15 15q11.2 loss - - CNVs Only Present In Patients; Zhang Y, 2015
AutCNV0004971 15 - gain - - CNVs Only Present In Patients; Bacchelli E, 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
AutCNV0005080 15 15q11.2 loss - - CNVs Only Present In Patients; Significant Enriched CNVs; Siu WK, 2016
AutCNV0005081 15 15q23q24.1 loss - - CNVs Only Present In Patients; Significant Enriched CNVs; Siu WK, 2016
AutCNV0005096 15 15q11.2q13.1 gain 1 - CNVs Only Present In Patients; Riikonen RS, 2016
AutCNV0005109 15 - loss 1 1 CNVs Only Present In Patients; Nava C, 2015
AutCNV0005115 15 15q11.2 loss - - CNVs Only Present In Patients; Kanduri C, 2016
AutCNV0005116 15 15q11.2 gain - - CNVs Only Present In Patients; Kanduri C, 2016
AutCNV0005117 15 15q13.2q13.3 loss - - CNVs Only Present In Patients; Kanduri C, 2016

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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