AP BIOLOGY

Detailed explanation-1: -Overview. Chromosome 1p deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the short arm (p) of chromosome 1. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved.

Detailed explanation-2: -The chromosomes in a homologous pair each have the same genes in the same order, but there may be variation between them, resulting in different alleles.

Detailed explanation-3: -Homologous chromosomes are chromosomes that share: The same structural features (e.g. same size, same banding patterns, same centromere positions) The same genes at the same loci positions (while the genes are the same, alleles may be different)

Detailed explanation-4: -Homologous chromosomes correspond to the chromosomes present on the same pair in contrast to non-homologous chromosomes where they are found on different pairs. Number of chromosomes in homologous pairs are based on the ploidy of that entity.