What is the result of a karyotype analysis?

A karyotype analysis involves examining the number and structure of chromosomes in a cell. This technique allows scientists to visualize the complete set of chromosomes, typically arranged in pairs by size and shape, which helps in identifying chromosomal abnormalities such as aneuploidy (an abnormal number of chromosomes) or structural changes like deletions, duplications, or translocations.

In a karyotype, each chromosome is stained to produce a characteristic banding pattern, making it easier to distinguish between the different chromosomes and identify any potential issues. This process is particularly useful in diagnosing genetic disorders that are caused by these chromosomal anomalies, as well as in prenatal screening.

Options relating to gene expression levels, assessment of specific genetic diseases, or mapping of genetic traits pertain to different genetic analyses and methodologies that are outside the scope of what a karyotype directly provides. Karyotype analysis focuses solely on the physical properties of chromosomes rather than their functional aspects or specific genetic characteristics.