A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819272



Internal ID15237237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6600566..6600853hg38UCSC Ensembl
Innerchr11:6621796..6622083hg19UCSC Ensembl
Innerchr11:6578372..6578659hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38288
hg19288
hg18288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419714
SamplesAK1
Known GenesRRP8
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)nsv819272
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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