AutismKB 2.0

View CNVs/SVs


View by Evidence Type: CNVs Only Present In Patients ( 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:16 ( 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
AutCNV0005001 16 16q12.2 loss - - CNVs Only Present In Patients; Al-Mamari W, 2015
AutCNV0005025 16 16p11.2 loss - - CNVs Only Present In Patients; de novo CNVs; Eriksson MA, 2015
AutCNV0005026 16 16p11.2 loss - - CNVs Only Present In Patients; Eriksson MA, 2015
AutCNV0005027 16 16p11.2 loss - - CNVs Only Present In Patients; de novo CNVs; Eriksson MA, 2015
AutCNV0005028 16 16p11.2 gain - - CNVs Only Present In Patients; Eriksson MA, 2015
AutCNV0005036 16 16p11.2 loss - - CNVs Only Present In Patients; Berman JI, 2015
AutCNV0005049 16 16p12.3 loss - - CNVs Only Present In Patients; Jiménez-Barrón LT, 2015
AutCNV0005052 16 16p11.2 loss - - CNVs Only Present In Patients; Duyzend MH, 2016
AutCNV0005053 16 16p11.2 gain - - CNVs Only Present In Patients; Duyzend MH, 2016
AutCNV0005054 16 16p11.2 loss - - CNVs Only Present In Patients; de novo CNVs; Duyzend MH, 2016
AutCNV0005079 16 16p13.11 gain - - CNVs Only Present In Patients; Significant Enriched CNVs; Siu WK, 2016
AutCNV0005082 16 16p13.11 gain - - CNVs Only Present In Patients; Significant Enriched CNVs; Siu WK, 2016
AutCNV0005083 16 16p13.11 gain - - CNVs Only Present In Patients; Significant Enriched CNVs; Siu WK, 2016
AutCNV0005086 16 16p13.11 gain - - CNVs Only Present In Patients; Significant Enriched CNVs; Siu WK, 2016
AutCNV0005107 16 16p11.2 gain - - CNVs Only Present In Patients; de novo CNVs; Nava C, 2015
AutCNV0005118 16 16p13.3 gain - - CNVs Only Present In Patients; Kanduri C, 2016
AutCNV0005138 16 16p11.2 gain - - CNVs Only Present In Patients; de novo CNVs; Soueid J, 2016
AutCNV0005159 16 16p13.11 gain - - CNVs Only Present In Patients; Pinto AM, 2015
AutCNV0005161 16 16p13.11 gain 1 - CNVs Only Present In Patients; Brownstein CA, 2016
AutCNV0005629 16 16 - - - CNVs Only Present In Patients; Krumm N, 2015
AutCNV0005646 16 16 - - - CNVs Only Present In Patients; Krumm N, 2015
AutCNV0005699 16 - Loss - - CNVs Only Present In Patients; de novo CNVs; Yuen RK, 2016
AutCNV0005735 16 - Gain - - CNVs Only Present In Patients; C Yuen RK, 2017
AutCNV0005736 16 - Gain - - CNVs Only Present In Patients; C Yuen RK, 2017
AutCNV0005765 16 - Gain - - CNVs Only Present In Patients; C Yuen RK, 2017

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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