A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979089



Internal ID12979619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98899360..98934460hg38UCSC Ensembl
Innerchr11:98770090..98805190hg19UCSC Ensembl
Innerchr11:98275300..98310400hg18UCSC Ensembl
Innerchr11:98275300..98310400hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3835101
hg1935101
hg1835101
hg1735101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35016
Supporting Variants
SamplesNA12891
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979089
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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