A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv775197



Internal ID15722467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55626700hg38UCSC Ensembl
Innerchr11:55367889..55394176hg19UCSC Ensembl
Innerchr11:55124465..55150752hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3826288
hg1926288
hg1826288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554818
Supporting Variants
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv775197
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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