A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819292



Internal ID15237257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93703819..93706894hg38UCSC Ensembl
Innerchr11:93436985..93440060hg19UCSC Ensembl
Innerchr11:93076633..93079708hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383076
hg193076
hg183076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419505
SamplesAK1
Known GenesKIAA1731
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)nsv819292
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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