Variant Details

Variant: esv2760036

Internal ID

9635495

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr15:68245734..68522324	hg38	UCSC Ensembl
Inner	chr15:68538072..68814663	hg19	UCSC Ensembl
Inner	chr15:66325126..66601717	hg18	UCSC Ensembl
Inner	chr15:66325126..66601717	hg17	UCSC Ensembl

Cytoband

15q23

Allele length

Assembly	Allele length
hg38	276591
hg19	276592
hg18	276592
hg17	276592

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv2758384

Samples

NA18991

Known Genes

FEM1B, ITGA11

Method

BAC aCGH

Analysis

Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).

Platform

Agilent

Comments

Reference

Redon_et_al_2006

Pubmed ID

17122850

Accession Number(s)

esv2760036

Frequency

Sample Size	270
Observed Gain	0
Observed Loss	1
Observed Complex	0
Frequency	n/a