A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799801



Internal ID18823484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55600413..55631424hg38UCSC Ensembl
Innerchr11:55367889..55398900hg19UCSC Ensembl
Innerchr11:55124465..55155476hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3831012
hg1931012
hg1831012
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892008
Supporting Variants
Samples
Known GenesOR4C11
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799801
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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