A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011297



Internal ID7060059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:79338115..79350089hg38UCSC Ensembl
Outerchr11:79049160..79061134hg19UCSC Ensembl
Outerchr11:78726808..78738782hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3811975
hg1911975
hg1811975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565009
SamplesHuRef
Known GenesTENM4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011297
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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