Product Details

Assay Reference Genome
Location

Chr.11:99037243 on build GRCh38
Cytoband
11q22.1
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
53942
Gene Symbol
CNTN5
Gene Name
contactin 5
Gene Aliases
HNB-2s, NB-2
Location
Chr.11:99020904-100358885 on build GRCh38
Assay Gene Location
Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
CNTN5 NM_001243270.1 NP_001230199.1
NM_001243271.1 NP_001230200.1
NM_014361.3 NP_055176.1
XM_011542871.1 XP_011541173.1
XM_011542873.1 XP_011541175.1
XM_017017926.1 XP_016873415.1
XM_017017927.1 XP_016873416.1
XM_017017928.1 XP_016873417.1
XM_017017929.1 XP_016873418.1
AK308788.1
BC039255.1 AAH39255.1
BC130619.1
BC144185.1
BC144186.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv428265 Chr11:98936705 - 99229707 on Build GRCh38 Loss CNTN5
nsv556046 Chr11:99024489 - 99058829 on Build GRCh38 Loss CNTN5
nsv832242 Chr11:98893493 - 99087654 on Build GRCh38 Loss CNTN5

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