I am reading a journal paper where the researchers are studying the effect of disease-causing mutations in the IL1RAPL1 gene. In the first figure of this paper, they show pedigrees of families where they have family members with the disease-causing mutations.
For the BMC family, they found using a SNP array that a deletion of ~200 kb between intron 5 and 6 of the IL1RAPL1 gene results in an in-frame deletion of exon 6.
I am having trouble interpreting the graph in Figure D, which is the results of the SNP array analysis. Aren't SNP arrays used for detecting single nucleotide polymorphisms? I am confused because in this paper they are using a SNP array to detect a gene deletion.
Any insights are appreciated.