A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992756



Internal ID7062249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2042513..2070610hg38UCSC Ensembl
Innerchr11:2063743..2091840hg19UCSC Ensembl
Innerchr11:2020319..2048416hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3828098
hg1928098
hg1828098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587102
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992756
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer