Variant Details

Variant: essv4541431

Internal ID

7127063

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr7:36486850..36486999	hg38	UCSC Ensembl
Outer	chr7:36486656..36487213	hg38	UCSC Ensembl
Inner	chr7:36526459..36526608	hg19	UCSC Ensembl
Outer	chr7:36526265..36526822	hg19	UCSC Ensembl
Inner	chr7:36492984..36493133	hg18	UCSC Ensembl
Outer	chr7:36492790..36493347	hg18	UCSC Ensembl

Cytoband

7p14.2

Allele length

Assembly	Allele length
hg38	558
hg19	558
hg18	558

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv1930825

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)

essv4541431

Frequency

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