Variant Details

Variant: essv4661277

Internal ID

7246909

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr17:50701106..50701148	hg38	UCSC Ensembl
Outer	chr17:50700916..50701342	hg38	UCSC Ensembl
Inner	chr17:48778467..48778509	hg19	UCSC Ensembl
Outer	chr17:48778277..48778703	hg19	UCSC Ensembl
Inner	chr17:46133466..46133508	hg18	UCSC Ensembl
Outer	chr17:46133276..46133702	hg18	UCSC Ensembl

Cytoband

17q21.33

Allele length

Assembly	Allele length
hg38	427
hg19	427
hg18	427

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2242752

Supporting Variants

Samples

NA18507

Known Genes

ANKRD40

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)

essv4661277

Frequency

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