A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892007



Internal ID18839717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55615681..55641224hg38UCSC Ensembl
Outerchr11:55600413..55660224hg38UCSC Ensembl
Innerchr11:55383157..55408700hg19UCSC Ensembl
Outerchr11:55367889..55427700hg19UCSC Ensembl
Innerchr11:55139733..55165276hg18UCSC Ensembl
Outerchr11:55124465..55184276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3859812
hg1959812
hg1859812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782818, essv25786837, essv25780072, essv25779495, essv25782279, essv25784559, essv25781282, essv25786396, essv25796929, essv25783522, essv25784497, essv25782330, essv25782194, essv25786559, essv25785149, essv25781541, essv25780246, essv25781962, essv25784933, essv25784227, essv25798378, essv25800594, essv25783738, essv25799918, essv25785314, essv25780144, essv25800322, essv25785345, essv25780137, essv25782600, essv25784282, essv25797640, essv25781254, essv25782349, essv25800311, essv25781998, essv25787008, essv25783175, essv25781455, essv25782012, essv25782250, essv25780845, essv25780320, essv25782359, essv25778520, essv25785370, essv25782160, essv25783309, essv25780220, essv25781078, essv25800683, essv25800141, essv25799828, essv25800744, essv25780797, essv25783131, essv25799866, essv25783531
Samples
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892007
Frequency
Sample Size3017
Observed Gain0
Observed Loss58
Observed Complex0
Frequencyn/a


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