A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763566



Internal ID15710836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:766479..870446hg38UCSC Ensembl
Innerchr11:766479..870446hg19UCSC Ensembl
Innerchr11:756479..860446hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38103968
hg19103968
hg18103968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552871
Supporting Variants
Samples
Known GenesCD151, CEND1, CHID1, EFCAB4A, NS3BP, PDDC1, PIDD, PNPLA2, POLR2L, RPLP2, SLC25A22, SNORA52, TSPAN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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