A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554934



Internal ID15995657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55607522..55685447hg38UCSC Ensembl
Innerchr11:55374998..55452923hg19UCSC Ensembl
Innerchr11:55131574..55209499hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3877926
hg1977926
hg1877926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv776598, nssv776597, nssv776596
Samples
Known GenesOR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554934
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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