A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv775922



Internal ID15723192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602150..55692619hg38UCSC Ensembl
Innerchr11:55369626..55460095hg19UCSC Ensembl
Innerchr11:55126202..55216671hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3890470
hg1990470
hg1890470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554861
Supporting Variants
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv775922
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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