Variant Details

Variant: esv2758351

Internal ID

9980428

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr14:27595893..27974036	hg38	UCSC Ensembl
Inner	chr14:28065099..28443242	hg19	UCSC Ensembl
Inner	chr14:27134939..27513082	hg18	UCSC Ensembl
Inner	chr14:27134939..27513082	hg17	UCSC Ensembl

Cytoband

14q12

Allele length

Assembly	Allele length
hg38	378144
hg19	378144
hg18	378144
hg17	378144

Variant Type

CNV gain+loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2759977

Supporting Variants

essv5328, essv2878, essv3411, essv7011, essv15512, essv1844, essv20056

Samples

NA18563, NA07048, NA18976, NA18945, NA18953, NA18505, NA18612

Known Genes

LINC00645

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)

esv2758351

Frequency

Sample Size	270
Observed Gain	5
Observed Loss	2
Observed Complex	0
Frequency	n/a