Assay Details
Target Gene Details
Entrez Gene ID: | 10752 |
Gene Name: | cell adhesion molecule L1 like |
Gene Aliases: |
CALL, L1CAM2 |
Location: |
Chr.3:196588-409417 on Build GRCh38 |
Assay Gene Location: | Within Intron 21 |
Target Gene Details
Entrez Gene ID: | 101927193 |
Gene Name: | CHL1 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.3:363373-385795 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CHL1-AS1 | NR_110739.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1010970 | Chr.3:188327 - 1623352 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() ![]() |
esv2759122 | Chr.3:29482 - 756820 on Build GRCh38 | Gain+Loss |
![]() ![]() ![]() ![]() |
nsv526340 | Chr.3:21733 - 2305176 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
esv3594901 | Chr.3:328751 - 540780 on Build GRCh38 | Gain |
![]() ![]() |
esv2667629 | Chr.3:39576 - 1039187 on Build GRCh38 | Deletion |
![]() ![]() ![]() ![]() ![]() |
nsv589291 | Chr.3:278518 - 1087112 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() |
nsv589293 | Chr.3:356048 - 433324 on Build GRCh38 | Loss |
![]() ![]() |
nsv1005290 | Chr.3:247092 - 949319 on Build GRCh38 | Loss |
![]() ![]() ![]() |
nsv834589 | Chr.3:235505 - 395503 on Build GRCh38 | Gain |
![]() ![]() |
dgv4608n100 | Chr.3:18655 - 438490 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() |
nsv1015041 | Chr.3:359178 - 529515 on Build GRCh38 | Gain |
![]() ![]() |
esv2763731 | Chr.3:243604 - 1386714 on Build GRCh38 | Gain+Loss |
![]() ![]() ![]() ![]() |
nsv1004600 | Chr.3:244100 - 607771 on Build GRCh38 | Loss |
![]() ![]() ![]() |
dgv4613n100 | Chr.3:52474 - 1799230 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() ![]() |
nsv589242 | Chr.3:47730 - 388999 on Build GRCh38 | Gain |
![]() ![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs75486561] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
![]() ![]() ![]() ![]() |
Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)