A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053742



Internal ID19142961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81274905..81306208hg38UCSC Ensembl
Innerchr11:80985948..81017251hg19UCSC Ensembl
Innerchr11:80663596..80694899hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3831304
hg1931304
hg1831304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n100
Supporting Variantsnssv3513113, nssv3509968, nssv3522277, nssv3504376, nssv3518973, nssv3504510, nssv3504040, nssv3511111, nssv3518585, nssv3509934, nssv3522433, nssv3515526, nssv3516820, nssv3516761, nssv3506422
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053742
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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