A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554935



Internal ID15995658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55607522..55692619hg38UCSC Ensembl
Innerchr11:55374998..55460095hg19UCSC Ensembl
Innerchr11:55131574..55216671hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3885098
hg1985098
hg1885098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1916n54
Supporting Variantsnssv776599
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)nsv554935
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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