A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470334



Internal ID15038473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55604331..55606227hg38UCSC Ensembl
Innerchr11:55371807..55373703hg19UCSC Ensembl
Innerchr11:55128383..55130279hg18UCSC Ensembl
Innerchr11:55147167..55149063hg16UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg381897
hg191897
hg181897
hg161897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438185
Supporting Variants
SamplesNA12763
Known GenesOR4C11
MethodSNP array
AnalysisNull genotypes - for each genotype assay and population sample we defined the null genotype pattern of that assay as the binary vector (length 90) of null genotype calls across the 90 individuals.
PlatformNot reported
Comments
ReferenceMcCarroll_et_al_2006
Pubmed ID16468122
Accession Number(s)nssv470334
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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