A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779845



Internal ID15727115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82897142..82969697hg38UCSC Ensembl
Innerchr11:82608184..82680739hg19UCSC Ensembl
Innerchr11:82285832..82358387hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3872556
hg1972556
hg1872556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555603
Supporting Variants
Samples
Known GenesC11orf82, PRCP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv779845
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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