Variant Details

Variant: esv1978078

Internal ID

7649189

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chrX:71903383..71903698	hg38	UCSC Ensembl
Outer	chrX:71903187..71903871	hg38	UCSC Ensembl
Inner	chrX:71123233..71123548	hg19	UCSC Ensembl
Outer	chrX:71123037..71123721	hg19	UCSC Ensembl
Inner	chrX:71039958..71040273	hg18	UCSC Ensembl
Outer	chrX:71039762..71040446	hg18	UCSC Ensembl

Cytoband

Xq13.1

Allele length

Assembly	Allele length
hg38	685
hg19	685
hg18	685

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4738916

Samples

NA18507

Known Genes

Method

Sequencing

Analysis

Hierarchical clustering of anomalous readpairs was used to identify groupings of five or more readpairs that had a similar size and position. Read pairs were defined as anomalous if they had high-confidence alignments of each individual read that nevertheless were either incorrectly oriented or implied an insert size of at least 3 standard deviations outside the sample median.

Platform

Not specified

Comments

Reference

Bentley_et_al_2008

Pubmed ID

18987734

Accession Number(s)

esv1978078

Frequency

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