Variant Details

Variant: esv2152466

Internal ID

7823577

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr14:104905189..104905430	hg38	UCSC Ensembl
Outer	chr14:104905018..104905569	hg38	UCSC Ensembl
Inner	chr14:105371526..105371767	hg19	UCSC Ensembl
Outer	chr14:105371355..105371906	hg19	UCSC Ensembl
Inner	chr14:104442571..104442812	hg18	UCSC Ensembl
Outer	chr14:104442400..104442951	hg18	UCSC Ensembl

Cytoband

14q32.33

Allele length

Assembly	Allele length
hg38	552
hg19	552
hg18	552

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4738374

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)

esv2152466

Frequency

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