A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175193



Internal ID15526128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55677392hg38UCSC Ensembl
Innerchr11:55371021..55444868hg19UCSC Ensembl
Innerchr11:55127597..55201444hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3873848
hg1973848
hg1873848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554896
Supporting Variants
SamplesHGDP00047
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)nssv1175193
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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