A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553173



Internal ID15993896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4566710..4668512hg38UCSC Ensembl
Innerchr11:4587940..4689742hg19UCSC Ensembl
Innerchr11:4544516..4646318hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38101803
hg19101803
hg18101803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1586n54
Supporting Variantsnssv764666
Samples
Known GenesC11orf40, OR51D1, OR51E1, OR52I1, OR52I2, TRIM68
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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