A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469559



Internal ID15187588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58963312..59120166hg38UCSC Ensembl
Innerchr11:58730785..58887639hg19UCSC Ensembl
Innerchr11:58487361..58644215hg18UCSC Ensembl
Innerchr11:58506145..58662999hg16UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38156855
hg19156855
hg18156855
hg16156855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675470, nssv1675620
Samples
Known GenesFAM111B, LOC283194
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nsv469559
Frequency
Sample Size265
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer