A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547881



Internal ID18402271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62450988..62451443hg38UCSC Ensembl
Outerchr11:62450926..62451555hg38UCSC Ensembl
Innerchr11:62218460..62218915hg19UCSC Ensembl
Outerchr11:62218398..62219027hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746628
Samples
Known GenesAHNAK
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547881
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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