A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995385



Internal ID7079808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66944478..66945945hg38UCSC Ensembl
Innerchr11:66711949..66713416hg19UCSC Ensembl
Innerchr11:66468525..66469992hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381468
hg191468
hg181468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586981
SamplesHuRef
Known GenesPC
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995385
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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