Assay Details
Target Gene Details
Entrez Gene ID: | 6664 |
Gene Name: | SRY-box 11 |
Gene Aliases: |
MRD27 |
Location: |
Chr.2:5692667-5701385 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SOX11 | NM_003108.3 | 1 | 4738 | NP_003099.1 |
| AB028641.1 | 1 | 4738 | BAA88122.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833292 | Chr.2:5663369 - 5827989 on Build GRCh38 | Gain+Loss |
|
| dgv609n67 | Chr.2:5665874 - 5710795 on Build GRCh38 | Gain |
|
| dgv608n67 | Chr.2:5647093 - 5731885 on Build GRCh38 | Gain |
|
| nsv953442 | Chr.2:5690269 - 5697668 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs112726300] 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