Variant Details

Variant: esv2758350

Internal ID

9980427

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr14:25758674..25935912	hg38	UCSC Ensembl
Inner	chr14:26227880..26405118	hg19	UCSC Ensembl
Inner	chr14:25297720..25474958	hg18	UCSC Ensembl
Inner	chr14:25297720..25474958	hg17	UCSC Ensembl

Cytoband

14q12

Allele length

Assembly	Allele length
hg38	177239
hg19	177239
hg18	177239
hg17	177239

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2759975

Supporting Variants

essv17771, essv16217, essv1852, essv20031, essv7160, essv5236, essv4757, essv24382, essv22515, essv3374, essv15129, essv24086, essv23472, essv19688, essv3020

Samples

NA18547, NA07048, NA10831, NA19161, NA18976, NA18981, NA12264, NA12707, NA18945, NA11882, NA10859, NA19129, NA18624, NA07034, NA18620

Known Genes

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)

esv2758350

Frequency

Sample Size	270
Observed Gain	15
Observed Loss	0
Observed Complex	0
Frequency	n/a