A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819457



Internal ID15584158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128812455..128813563hg38UCSC Ensembl
Innerchr11:128682350..128683458hg19UCSC Ensembl
Innerchr11:128187560..128188668hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381109
hg191109
hg181109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419174
SamplesAK1
Known GenesFLI1
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)nsv819457
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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