Variant Details

Variant: nsv469823

Internal ID

15534538

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr9:64476875..64698199	hg38	UCSC Ensembl
Inner	chr9:69489293..69710617	hg19	UCSC Ensembl
Inner	chr9:68779113..69000437	hg18	UCSC Ensembl
Inner	chr9:65619734..65841058	hg16	UCSC Ensembl

Cytoband

9q12

Allele length

Assembly	Allele length
hg38	221325
hg19	221325
hg18	221325
hg16	221325

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

nssv1676036, nssv1673849

Samples

Known Genes

LOC100133920

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)

nsv469823

Frequency

Sample Size	265
Observed Gain	2
Observed Loss	0
Observed Complex	0
Frequency	n/a