A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764667



Internal ID15711937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4571488..4661146hg38UCSC Ensembl
Innerchr11:4592718..4682376hg19UCSC Ensembl
Innerchr11:4549294..4638952hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3889659
hg1989659
hg1889659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553174
Supporting Variants
Samples
Known GenesC11orf40, OR51D1, OR51E1, OR52I1, OR52I2, TRIM68
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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