A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25793003



Internal ID18823309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55679951hg38UCSC Ensembl
Innerchr11:55367889..55447427hg19UCSC Ensembl
Innerchr11:55124465..55204003hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3879539
hg1979539
hg1879539
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=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25793003
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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