A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555965



Internal ID16343374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93980745..94014569hg38UCSC Ensembl
Innerchr11:93713911..93747735hg19UCSC Ensembl
Innerchr11:93353559..93387383hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3833825
hg1933825
hg1833825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781561
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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