A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174655



Internal ID15509128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55592737..55692619hg38UCSC Ensembl
Innerchr11:55360213..55460095hg19UCSC Ensembl
Innerchr11:55116789..55216671hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3899883
hg1999883
hg1899883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554813
Supporting Variants
Samples1787431166_A
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)nssv1174655
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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