Assay Details
Target Gene Details
Entrez Gene ID: | 57834 |
Gene Name: | cytochrome P450 family 4 subfamily F member 11 |
Gene Aliases: |
CYPIVF11 |
Location: |
Chr.19:15912370-15934866 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CYP4F11 | NM_001128932.1 | NP_001122404.1 | ||
| NM_021187.3 | NP_067010.3 | |||
| AF236085.1 | AAG15889.1 | |||
| AK125714.1 | ||||
| AK289424.1 | ||||
| AL833940.1 | CAD38795.2 | |||
| BC016853.1 | AAH16853.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2671181 | Chr.19:15768634 - 15926128 on Build GRCh38 | Deletion |
|
| esv3334671 | Chr.19:15673766 - 15931354 on Build GRCh38 | Duplication |
|
| nsv833766 | Chr.19:15759095 - 15956904 on Build GRCh38 | Loss |
|
| nsv1064684 | Chr.19:15311319 - 16062011 on Build GRCh38 | Gain |
|
| esv2718244 | Chr.19:15743561 - 15951200 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs74957415] 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: |
|

Genomic Map