A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438185



Internal ID15041416
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 StatusM
Merged Variants
Supporting Variantsnssv470334, nssv470333, nssv470332, nssv470331
SamplesNA12763, NA12864, NA11832, NA12003
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)nsv438185
Frequency
Sample Size269
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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