Variant Details

Variant: essv4956741

Internal ID

7542373

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr7:45432541..45432730	hg38	UCSC Ensembl
Outer	chr7:45432473..45432798	hg38	UCSC Ensembl
Inner	chr7:45472140..45472329	hg19	UCSC Ensembl
Outer	chr7:45472072..45472397	hg19	UCSC Ensembl
Inner	chr7:45438665..45438854	hg18	UCSC Ensembl
Outer	chr7:45438597..45438922	hg18	UCSC Ensembl

Cytoband

7p12.3

Allele length

Assembly	Allele length
hg38	326
hg19	326
hg18	326

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2243668

Supporting Variants

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)

essv4956741

Frequency

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