A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819971



Internal ID15584672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59664247..59667093hg38UCSC Ensembl
Innerchr11:59431720..59434566hg19UCSC Ensembl
Innerchr11:59188296..59191142hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382847
hg192847
hg182847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419482
SamplesAK1
Known GenesPATL1
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)nsv819971
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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