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: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
AutCNV0004826 16 16p12.2p11.2 loss - - CNVs Only Present In Patients; de novo CNVs; Okamoto N, 2014
AutCNV0004827 16 16p12.2p11.2 gain - - CNVs Only Present In Patients; de novo CNVs; Okamoto N, 2014
AutCNV0004838 16 16p13.3 loss - - CNVs Only Present In Patients; de novo CNVs; Asadollahi R, 2014
AutCNV0004843 16 16p13.3 loss - - CNVs Only Present In Patients; de novo CNVs; Asadollahi R, 2014
AutCNV0004854 16 16p11.2 gain - - CNVs Only Present In Patients; Moreira DP, 2014
AutCNV0004855 16 16p11.2 gain - - CNVs Only Present In Patients; Moreira DP, 2014
AutCNV0004856 16 16p11.2 gain - - CNVs Only Present In Patients; de novo CNVs; Moreira DP, 2014
AutCNV0004857 16 16p11.2 gain - - CNVs Only Present In Patients; Moreira DP, 2014
AutCNV0004858 16 16p11.2 loss - - CNVs Only Present In Patients; Moreira DP, 2014
AutCNV0004870 16 16p13.11 loss 13 - CNVs Only Present In Patients; Gümü?lü KE, 2015
AutCNV0004871 16 16p11.2 loss 12 - CNVs Only Present In Patients; Gümü?lü KE, 2015
AutCNV0004877 16 16p13.3 loss 2 - CNVs Only Present In Patients; Overlapping/Recurrent CNVs; Gümü?lü KE, 2015
AutCNV0004882 16 16q24.1 gain - - CNVs Only Present In Patients; Dharmadhikari AV, 2014
AutCNV0004883 16 16q23.3 gain - - CNVs Only Present In Patients; Dharmadhikari AV, 2014
AutCNV0004884 16 16q24.1 gain - - CNVs Only Present In Patients; Dharmadhikari AV, 2014
AutCNV0004885 16 16q24.2 gain - - CNVs Only Present In Patients; Dharmadhikari AV, 2014
AutCNV0004886 16 16q24.1 gain - - CNVs Only Present In Patients; Dharmadhikari AV, 2014
AutCNV0004887 16 16q24.1 gain - - CNVs Only Present In Patients; Dharmadhikari AV, 2014
AutCNV0004888 16 16q24.1 gain - - CNVs Only Present In Patients; Dharmadhikari AV, 2014
AutCNV0004919 16 - loss - - CNVs Only Present In Patients; de novo CNVs; Tammimies K, 2015
AutCNV0004923 16 - gain - - CNVs Only Present In Patients; Tammimies K, 2015
AutCNV0004927 16 - loss - - CNVs Only Present In Patients; Tammimies K, 2015
AutCNV0004928 16 - gain - - CNVs Only Present In Patients; Tammimies K, 2015
AutCNV0004969 16 16q24.1 loss 1 - CNVs Only Present In Patients; de novo CNVs; Smith AW, 2015
AutCNV0004982 16 16p11.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; Sanders SJ, 2015

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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