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
AutCNV0005122 15 15q23q24.1 loss - - CNVs Only Present In Patients; Siu WK, 2016
AutCNV0005505 15 15q13.3 gain - - Chilian B, 2013
AutCNV0005506 15 15q13.3 loss - - Chilian B, 2013
AutCNV0005627 15 15 gain - - CNVs Only Present In Patients; Mercati O, 2017
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
AutCNV0005657 15 15 - - - Krumm N, 2015
AutCNV0005665 15 15 - - - Krumm N, 2015
AutCNV0005734 15 - Gain - - CNVs Only Present In Patients; C Yuen RK, 2017
AutCNV0005781 15 15q11.2 Loss - - Kalsner L, 2018
AutCNV0005791 15 15q14 Gain - - Kalsner L, 2018
AutCNV0005848 15 15q21.3 Loss - - Egger G, 2014
AutCNV0005869 15 15q11.2 Gain - - Alvarez-Mora MI, 2016
AutCNV0005871 15 15q11.2 Gain - - Alvarez-Mora MI, 2016
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
AutCNV0005943 15 15q11.2 loss - - Brandler WM, 2018
AutCNV0005944 15 15q11.2-q13.1 gain - - 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