A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175163



Internal ID15531632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55674892hg38UCSC Ensembl
Innerchr11:55371021..55442368hg19UCSC Ensembl
Innerchr11:55127597..55198944hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3871348
hg1971348
hg1871348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554895
Supporting Variants
SamplesHGDP01180
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)nssv1175163
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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