A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796929



Internal ID18826815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55660224hg38UCSC Ensembl
Innerchr11:55367889..55427700hg19UCSC Ensembl
Innerchr11:55124465..55184276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3859812
hg1959812
hg1859812
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892007
Supporting Variants
Samples
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796929
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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