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MAXImum [283]
3 years ago
14

How can karyotype analysis detect genetic disorders lab 12-2 answers?

Biology
2 answers:
timama [110]3 years ago
7 0

 Karyotype enable viewing of the physical attributes of chromosomes. When compared to the karyotype of a normal individual, any abnormalities in chromosomes can be identified by either noticing an abnormal number of chromosomes or pairing (aneuploidy), or regional changes within chromosomes such as shorter or longer than normal chromosomes due to translocations.






Degger [83]3 years ago
6 0
<h2>Answer:</h2>
  • Karyotype is the image or a visual aid which present the pair and order of all the chromosome in an organism.
  • <em><u>An analyst can detect genetic disorder by comparing that karyotype with the normal person karyotype</u></em>.
  • Now he can locate the difference either in number of chromosomes or in the structure of chromosome.
  • Through looking at karyotype he can tell number of chromosome having abnormality.

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If there are 100 individuals in a population and 20 are homozygous for b, 60 are heterozygous, and 20 are homozygous for b, the allele frequency of b is 50%.  

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If an allele is found in a population on I chromosomes, the allele frequency is the proportion of all I occurrences of that allele to the total number of copies of the chromosome in the population (nN). Despite being related, the genotype frequency and the allele frequency are separate and one can infer the other from the other.

To know more about allele please refer: brainly.com/question/7602134

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