Assay Details
Target Gene Details
Entrez Gene ID: | 26994 |
Gene Name: | ring finger protein 11 |
Gene Aliases: |
CGI-123, SID1669 |
Location: |
Chr.1:51236273-51273447 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RNF11 | NM_014372.4 | NP_055187.1 | ||
| AB024703.1 | BAA84683.1 | |||
| AF151881.1 | AAD34118.1 | |||
| AK293047.1 | ||||
| AK313140.1 | ||||
| BC020964.2 | AAH20964.1 | |||
| BC047654.1 | AAH47654.1 | |||
| DB265274.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3586032 | Chr.1:51252532 - 51257060 on Build GRCh38 | Loss |
|
| nsv945940 | Chr.1:51250600 - 51254219 on Build GRCh38 | Duplication |
|
| esv2663443 | Chr.1:51248373 - 51254630 on Build GRCh38 | Deletion |
|
| esv3586031 | Chr.1:51248392 - 51254652 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs72896491] 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