A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175188



Internal ID15506828
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
Samples1780854257_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)nssv1175188
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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