A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820233



Internal ID15238198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34149816..34152473hg38UCSC Ensembl
Innerchr11:34171363..34174020hg19UCSC Ensembl
Innerchr11:34127939..34130596hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382658
hg192658
hg182658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419458
SamplesAK1
Known GenesABTB2
MethodOligo aCGH
AnalysisThe array was scanned with Agilent DNA microarray scanner at 2 micron resolution. The resulting image was extracted by Agilent's Feature Extraction software. The log2 ratios were analyzed using NEXUS software. Each aberration call was manually checked to confirm the accuracy of the calls.
PlatformGSE19651
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nsv820233
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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