A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419133



Internal ID15236187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113768116..113769066hg38UCSC Ensembl
Innerchr11:113638838..113639788hg19UCSC Ensembl
Innerchr11:113144048..113144998hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38951
hg19951
hg18951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820035
Supporting Variants
SamplesAK1
Known GenesZW10
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)nssv1419133
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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