A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764494



Internal ID15711764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2291007..2312445hg38UCSC Ensembl
Innerchr11:2312237..2333675hg19UCSC Ensembl
Innerchr11:2268813..2290251hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3821439
hg1921439
hg1821439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553081
Supporting Variants
Samples
Known GenesC11orf21, TSPAN32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764494
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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