A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819020



Internal ID15238303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10558798..10560604hg38UCSC Ensembl
Innerchr11:10580345..10582151hg19UCSC Ensembl
Innerchr11:10536921..10538727hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381807
hg191807
hg181807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419332
SamplesAK1
Known GenesLYVE1, MRVI1-AS1
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)nsv819020
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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