A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778281



Internal ID18823556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55685447hg38UCSC Ensembl
Innerchr11:55367889..55452923hg19UCSC Ensembl
Innerchr11:55124465..55209499hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3885035
hg1985035
hg1885035
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892006
Supporting Variants
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778281
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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