Variant Details

Variant: nsv469879

Internal ID

15534594

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr9:42265932..42448162	hg38	UCSC Ensembl
Inner	chr9:41655561..41836911	hg19	UCSC Ensembl
Inner	chr9:41645561..41826911	hg18	UCSC Ensembl
Inner	chr9:41840000..42021335	hg16	UCSC Ensembl

Cytoband

9p12

Allele length

Assembly	Allele length
hg38	182231
hg19	181351
hg18	181351
hg16	181336

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

nssv1676208, nssv1676237, nssv1673612, nssv1672589

Samples

Known Genes

Method

BAC aCGH

Analysis

A 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.

Platform

GPL4010

Comments

Reference

Locke_et_al_2006

Pubmed ID

16826518

Accession Number(s)

nsv469879

Frequency

Sample Size	265
Observed Gain	4
Observed Loss	0
Observed Complex	0
Frequency	n/a