Variant Details

Variant: esv2368922

Internal ID

8040034

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr7:128669172..128669504	hg38	UCSC Ensembl
Outer	chr7:128669017..128669679	hg38	UCSC Ensembl
Inner	chr7:128309226..128309558	hg19	UCSC Ensembl
Outer	chr7:128309071..128309733	hg19	UCSC Ensembl
Inner	chr7:128096462..128096794	hg18	UCSC Ensembl
Outer	chr7:128096307..128096969	hg18	UCSC Ensembl

Cytoband

7q32.1

Allele length

Assembly	Allele length
hg38	663
hg19	663
hg18	663

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv39e194

Supporting Variants

essv4960846

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)

esv2368922

Frequency

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