A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892008



Internal ID18839718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55606497..55624962hg38UCSC Ensembl
Outerchr11:55600413..55631424hg38UCSC Ensembl
Innerchr11:55373973..55392438hg19UCSC Ensembl
Outerchr11:55367889..55398900hg19UCSC Ensembl
Innerchr11:55130549..55149014hg18UCSC Ensembl
Outerchr11:55124465..55155476hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3831012
hg1931012
hg1831012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800448, essv25785777, essv25799801, essv25796250
Samples
Known GenesOR4C11
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892008
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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