A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418685



Internal ID15582469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92985117..93005629hg38UCSC Ensembl
Innerchr11:92718283..92738795hg19UCSC Ensembl
Innerchr11:92357931..92378443hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3820513
hg1920513
hg1820513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820151
Supporting Variants
SamplesAK1
Known Genes
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)nssv1418685
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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