Variant Details

Variant: esv2759873

Internal ID

9635332

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:131562907..131879091	hg38	UCSC Ensembl
Inner	chr11:131432801..131748985	hg19	UCSC Ensembl
Inner	chr11:130938011..131254195	hg18	UCSC Ensembl
Inner	chr11:130938011..131254195	hg17	UCSC Ensembl

Cytoband

11q25

Allele length

Assembly	Allele length
hg38	316185
hg19	316185
hg18	316185
hg17	316185

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv2758289

Samples

NA19222, NA19173, NA19093, NA18603, NA06993, NA19210, NA11839, NA11840, NA18856, NA19206, NA19238, NA19131, NA19101, NA19128, NA19205, NA18913

Known Genes

NTM

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)

esv2759873

Frequency

Sample Size	270
Observed Gain	16
Observed Loss	0
Observed Complex	0
Frequency	n/a