A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5069255



Internal ID7813113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55685533hg38UCSC Ensembl
Innerchr11:55367889..55453009hg19UCSC Ensembl
Innerchr11:55124465..55209585hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3885121
hg1985121
hg1885121
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2421634
Supporting Variants
SamplesNA21383
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisTo assess copy number variation we merged and analysed the probe level intensity data from both the Affymetrix and Illumina arrays.
PlatformNot specified
Comments
ReferenceAltshuler_et_al_2010
Pubmed ID20811451
Accession Number(s)essv5069255
Frequency
Sample Size1184
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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