A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819435



Internal ID15237400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102704737..102705859hg38UCSC Ensembl
Innerchr11:102575468..102576590hg19UCSC Ensembl
Innerchr11:102080678..102081800hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381123
hg191123
hg181123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419178
SamplesAK1
Known GenesMMP27
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)nsv819435
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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