MOESM4 of Inter- and intra-breed genome-wide copy number diversity in a large cohort of European equine breeds

Additional file 4: Table S3. Genomic regions validated for CNVs by RT-qPCR. Primer sequences, position, product size, annealing temperature and TaqMan probes are shown. The CNV status in the SNP-array and in the qPCR and the CNV validation by qPCR are given. Table S4. Results of quantitative PCR. The results of the four CNVs per each horse and the outcome of the validation through qPCR are presented.

附加文件4：表S3。经RT-qPCR验证的拷贝数变异（Copy Number Variation, CNV）基因组区域。本表格列出了引物序列、引物结合位置、扩增产物长度、退火温度及TaqMan探针信息，同时提供了SNP芯片（Single Nucleotide Polymorphism array）与定量PCR（quantitative PCR, qPCR）检测中的CNV状态，以及经qPCR验证的CNV结果。表S4：定量PCR检测结果。本表格呈现了每匹马对应的4种CNV的检测结果，以及通过qPCR完成的CNV验证结果。