Variant Details

Variant: essv4616267

Internal ID

6855213

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr12:27281071..27281385	hg38	UCSC Ensembl
Outer	chr12:27280863..27281596	hg38	UCSC Ensembl
Inner	chr12:27434004..27434318	hg19	UCSC Ensembl
Outer	chr12:27433796..27434529	hg19	UCSC Ensembl
Inner	chr12:27325271..27325585	hg18	UCSC Ensembl
Outer	chr12:27325063..27325796	hg18	UCSC Ensembl

Cytoband

12p11.23

Allele length

Assembly	Allele length
hg38	734
hg19	734
hg18	734

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2395169

Supporting Variants

Samples

NA18507

Known Genes

STK38L

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)

essv4616267

Frequency

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