Product Details
- Assay Reference Genome
Location
Chr.11:46651362 on build GRCh38
- Cytoband
- 11p11.2
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs73451863] 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.
Target Gene Details
- Entrez Gene ID
- 9776
- Gene Symbol
- ATG13
- Gene Name
- autophagy related 13
- Gene Aliases
- KIAA0652, PARATARG8
- Location
- Chr.11:46617276-46676019 on build GRCh38
- Assay Gene Location
- Within Intron 12
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