A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800311



Internal ID18831105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55647540hg38UCSC Ensembl
Innerchr11:55367889..55415016hg19UCSC Ensembl
Innerchr11:55124465..55171592hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3847128
hg1947128
hg1847128
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892007
Supporting Variants
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800311
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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