A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819964



Internal ID15237929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10515707..10523988hg38UCSC Ensembl
Innerchr11:10537254..10545535hg19UCSC Ensembl
Innerchr11:10493830..10502111hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388282
hg198282
hg188282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419864
SamplesAK1
Known GenesRNF141
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)nsv819964
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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